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What is the type of genetic variation for RS1952480014 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1952480014 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1952480014 SNP? | The resulting gene consequence is a splice acceptor variant. | <s>[INST] What is the genetic molecular consequence for RS1952480014 SNP? [/INST] The resulting gene consequence is a splice acceptor variant. </s> |
Which condition is asociated with RS1060503074 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1060503074 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1060503074 SNP. | <s>[INST] Which condition is asociated with RS1060503074 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1060503074 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1060503074 SNP. </s> |
In which chromosome is RS1060503074 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1060503074 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1060503074 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1060503074 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1060503074 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS1060503074 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS1060503074 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1060503074 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1060503074 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1060503074 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1060503074 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1060503074 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1060503074 SNP? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for RS1060503074 SNP? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with RS1131690902 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1131690902 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1131690902 SNP. | <s>[INST] Which condition is asociated with RS1131690902 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1131690902 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1131690902 SNP. </s> |
In which chromosome is RS1131690902 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1131690902 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1131690902 SNP? | Associated methods are: research, clinical testing. | <s>[INST] Which methods support the evidence found for the RS1131690902 SNP? [/INST] Associated methods are: research, clinical testing. </s> |
What is the clinical significance of RS1131690902 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS1131690902 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS1131690902 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1131690902 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1131690902 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS1131690902 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS1131690902 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1131690902 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1131690902 SNP? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for RS1131690902 SNP? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with RS1948523741 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1948523741 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1948523741 SNP. | <s>[INST] Which condition is asociated with RS1948523741 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1948523741 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1948523741 SNP. </s> |
In which chromosome is RS1948523741 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1948523741 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1948523741 SNP? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the RS1948523741 SNP? [/INST] Associated methods are: research. </s> |
What is the clinical significance of RS1948523741 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS1948523741 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS1948523741 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1948523741 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1948523741 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS1948523741 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS1948523741 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1948523741 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1948523741 SNP? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for RS1948523741 SNP? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with RS1949360306 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1949360306 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1949360306 SNP. | <s>[INST] Which condition is asociated with RS1949360306 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1949360306 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1949360306 SNP. </s> |
In which chromosome is RS1949360306 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1949360306 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1949360306 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1949360306 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1949360306 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS1949360306 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS1949360306 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1949360306 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1949360306 SNP? | The origin is unknown. | <s>[INST] What is the origin for RS1949360306 SNP? [/INST] The origin is unknown. </s> |
What is the type of genetic variation for RS1949360306 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1949360306 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1949360306 SNP? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for RS1949360306 SNP? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with RS1952654925 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1952654925 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1952654925 SNP. | <s>[INST] Which condition is asociated with RS1952654925 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1952654925 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1952654925 SNP. </s> |
In which chromosome is RS1952654925 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1952654925 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1952654925 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1952654925 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1952654925 SNP, is it benign or pathogenic? | It is Uncertain significance. | <s>[INST] What is the clinical significance of RS1952654925 SNP, is it benign or pathogenic? [/INST] It is Uncertain significance. </s> |
How long is the variation length for RS1952654925 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1952654925 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1952654925 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1952654925 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1952654925 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1952654925 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1952654925 SNP? | The resulting gene consequence is a splice acceptor variant. | <s>[INST] What is the genetic molecular consequence for RS1952654925 SNP? [/INST] The resulting gene consequence is a splice acceptor variant. </s> |
Which condition is asociated with RS1952624973 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1952624973 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1952624973 SNP. | <s>[INST] Which condition is asociated with RS1952624973 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1952624973 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1952624973 SNP. </s> |
In which chromosome is RS1952624973 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1952624973 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1952624973 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1952624973 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1952624973 SNP, is it benign or pathogenic? | It is Uncertain significance. | <s>[INST] What is the clinical significance of RS1952624973 SNP, is it benign or pathogenic? [/INST] It is Uncertain significance. </s> |
How long is the variation length for RS1952624973 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1952624973 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1952624973 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1952624973 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1952624973 SNP? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for RS1952624973 SNP? [/INST] The variation is a Deletion. </s> |
What is the genetic molecular consequence for RS1952624973 SNP? | The resulting gene consequence is a splice acceptor variant. | <s>[INST] What is the genetic molecular consequence for RS1952624973 SNP? [/INST] The resulting gene consequence is a splice acceptor variant. </s> |
Which condition is asociated with SNV1062990? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsSNV1062990. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1062990. | <s>[INST] Which condition is asociated with SNV1062990? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsSNV1062990. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1062990. </s> |
In which chromosome is SNV1062990 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1062990 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1062990? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1062990? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1062990, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV1062990, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV1062990? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1062990? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1062990? | The origin is germline. | <s>[INST] What is the origin for SNV1062990? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1062990? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1062990? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1062990? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for SNV1062990? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with RS1131690886 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1131690886 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1131690886 SNP. | <s>[INST] Which condition is asociated with RS1131690886 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1131690886 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1131690886 SNP. </s> |
In which chromosome is RS1131690886 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1131690886 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1131690886 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1131690886 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1131690886 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS1131690886 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS1131690886 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1131690886 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1131690886 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1131690886 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1131690886 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1131690886 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1131690886 SNP? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for RS1131690886 SNP? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with SNV1062995? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsSNV1062995. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1062995. | <s>[INST] Which condition is asociated with SNV1062995? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsSNV1062995. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1062995. </s> |
In which chromosome is SNV1062995 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1062995 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1062995? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1062995? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1062995, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV1062995, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV1062995? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1062995? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1062995? | The origin is germline. | <s>[INST] What is the origin for SNV1062995? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1062995? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1062995? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1062995? | The resulting gene consequence is a splice acceptor variant. | <s>[INST] What is the genetic molecular consequence for SNV1062995? [/INST] The resulting gene consequence is a splice acceptor variant. </s> |
Which condition is asociated with SNV1062984? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsSNV1062984. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1062984. | <s>[INST] Which condition is asociated with SNV1062984? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsSNV1062984. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1062984. </s> |
In which chromosome is SNV1062984 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1062984 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1062984? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1062984? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1062984, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV1062984, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV1062984? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1062984? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1062984? | The origin is germline. | <s>[INST] What is the origin for SNV1062984? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1062984? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1062984? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1062984? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for SNV1062984? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with SNV1062989? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsSNV1062989. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1062989. | <s>[INST] Which condition is asociated with SNV1062989? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsSNV1062989. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1062989. </s> |
In which chromosome is SNV1062989 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1062989 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1062989? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1062989? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1062989, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV1062989, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV1062989? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1062989? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1062989? | The origin is germline. | <s>[INST] What is the origin for SNV1062989? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1062989? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1062989? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1062989? | The resulting gene consequence is a splice acceptor variant. | <s>[INST] What is the genetic molecular consequence for SNV1062989? [/INST] The resulting gene consequence is a splice acceptor variant. </s> |
Which condition is asociated with RS794727199 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS794727199 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS794727199 SNP. | <s>[INST] Which condition is asociated with RS794727199 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS794727199 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS794727199 SNP. </s> |
In which chromosome is RS794727199 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS794727199 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS794727199 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS794727199 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS794727199 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS794727199 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS794727199 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS794727199 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS794727199 SNP? | The origin is germline. | <s>[INST] What is the origin for RS794727199 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS794727199 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS794727199 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS794727199 SNP? | The resulting gene consequence is a splice acceptor variant. | <s>[INST] What is the genetic molecular consequence for RS794727199 SNP? [/INST] The resulting gene consequence is a splice acceptor variant. </s> |
Which condition is asociated with SNV1063000? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsSNV1063000. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1063000. | <s>[INST] Which condition is asociated with SNV1063000? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsSNV1063000. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1063000. </s> |
In which chromosome is SNV1063000 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1063000 located? [/INST] It is located in the chromosome 13. </s> |