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Which methods support the evidence found for the SNV2056034? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV2056034? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV2056034, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV2056034, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV2056034? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV2056034? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV2056034? | The origin is germline. | <s>[INST] What is the origin for SNV2056034? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV2056034? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV2056034? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV2056034? | The resulting gene consequence is a splice acceptor variant. | <s>[INST] What is the genetic molecular consequence for SNV2056034? [/INST] The resulting gene consequence is a splice acceptor variant. </s> |
Which condition is asociated with SNV1874620? | 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/RsSNV1874620. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1874620. | <s>[INST] Which condition is asociated with SNV1874620? [/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/RsSNV1874620. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1874620. </s> |
In which chromosome is SNV1874620 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1874620 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1874620? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1874620? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1874620, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV1874620, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV1874620? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1874620? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1874620? | The origin is germline. | <s>[INST] What is the origin for SNV1874620? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1874620? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1874620? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1874620? | The resulting gene consequence is a missense variant. | <s>[INST] What is the genetic molecular consequence for SNV1874620? [/INST] The resulting gene consequence is a missense variant. </s> |
Which condition is asociated with SNV1874613? | 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/RsSNV1874613. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1874613. | <s>[INST] Which condition is asociated with SNV1874613? [/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/RsSNV1874613. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1874613. </s> |
In which chromosome is SNV1874613 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1874613 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1874613? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1874613? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1874613, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV1874613, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV1874613? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1874613? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1874613? | The origin is germline. | <s>[INST] What is the origin for SNV1874613? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1874613? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1874613? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1874613? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for SNV1874613? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with RS1168863456 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/RsRS1168863456 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1168863456 SNP. | <s>[INST] Which condition is asociated with RS1168863456 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/RsRS1168863456 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1168863456 SNP. </s> |
In which chromosome is RS1168863456 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1168863456 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1168863456 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1168863456 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1168863456 SNP, is it benign or pathogenic? | It is Uncertain significance. | <s>[INST] What is the clinical significance of RS1168863456 SNP, is it benign or pathogenic? [/INST] It is Uncertain significance. </s> |
How long is the variation length for RS1168863456 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1168863456 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1168863456 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1168863456 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1168863456 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1168863456 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1168863456 SNP? | The resulting gene consequence is a missense variant. | <s>[INST] What is the genetic molecular consequence for RS1168863456 SNP? [/INST] The resulting gene consequence is a missense variant. </s> |
Which condition is asociated with RS896487590 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/RsRS896487590 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS896487590 SNP. | <s>[INST] Which condition is asociated with RS896487590 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/RsRS896487590 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS896487590 SNP. </s> |
In which chromosome is RS896487590 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS896487590 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS896487590 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS896487590 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS896487590 SNP, is it benign or pathogenic? | It is Benign. | <s>[INST] What is the clinical significance of RS896487590 SNP, is it benign or pathogenic? [/INST] It is Benign. </s> |
How long is the variation length for RS896487590 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS896487590 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS896487590 SNP? | The origin is germline. | <s>[INST] What is the origin for RS896487590 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS896487590 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS896487590 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS896487590 SNP? | The resulting gene consequence is a missense variant. | <s>[INST] What is the genetic molecular consequence for RS896487590 SNP? [/INST] The resulting gene consequence is a missense variant. </s> |
Which condition is asociated with RS769696726 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/RsRS769696726 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS769696726 SNP. | <s>[INST] Which condition is asociated with RS769696726 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/RsRS769696726 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS769696726 SNP. </s> |
In which chromosome is RS769696726 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS769696726 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS769696726 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS769696726 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS769696726 SNP, is it benign or pathogenic? | It is Benign. | <s>[INST] What is the clinical significance of RS769696726 SNP, is it benign or pathogenic? [/INST] It is Benign. </s> |
How long is the variation length for RS769696726 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS769696726 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS769696726 SNP? | The origin is germline. | <s>[INST] What is the origin for RS769696726 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS769696726 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS769696726 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS769696726 SNP? | The resulting gene consequence is a missense variant. | <s>[INST] What is the genetic molecular consequence for RS769696726 SNP? [/INST] The resulting gene consequence is a missense variant. </s> |
Which condition is asociated with RS387906521 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/RsRS387906521 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS387906521 SNP. | <s>[INST] Which condition is asociated with RS387906521 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/RsRS387906521 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS387906521 SNP. </s> |
In which chromosome is RS387906521 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS387906521 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS387906521 SNP? | Associated methods are: clinical testing, literature only. | <s>[INST] Which methods support the evidence found for the RS387906521 SNP? [/INST] Associated methods are: clinical testing, literature only. </s> |
What is the clinical significance of RS387906521 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS387906521 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS387906521 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS387906521 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS387906521 SNP? | The origin is germline. | <s>[INST] What is the origin for RS387906521 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS387906521 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS387906521 SNP? [/INST] The variation is a single nucleotide variant. </s> |
Which condition is asociated with RS137853294 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/RsRS137853294 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS137853294 SNP. | <s>[INST] Which condition is asociated with RS137853294 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/RsRS137853294 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS137853294 SNP. </s> |
In which chromosome is RS137853294 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS137853294 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS137853294 SNP? | Associated methods are: phenotyping only, research, clinical testing, literature only. | <s>[INST] Which methods support the evidence found for the RS137853294 SNP? [/INST] Associated methods are: phenotyping only, research, clinical testing, literature only. </s> |
What is the clinical significance of RS137853294 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS137853294 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS137853294 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS137853294 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS137853294 SNP? | The origin is germline. | <s>[INST] What is the origin for RS137853294 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS137853294 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS137853294 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS137853294 SNP? | The resulting gene consequence is a missense variant. | <s>[INST] What is the genetic molecular consequence for RS137853294 SNP? [/INST] The resulting gene consequence is a missense variant. </s> |
Which condition is asociated with RS587776788 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/RsRS587776788 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587776788 SNP. | <s>[INST] Which condition is asociated with RS587776788 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/RsRS587776788 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587776788 SNP. </s> |
In which chromosome is RS587776788 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587776788 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587776788 SNP? | Associated methods are: clinical testing, literature only. | <s>[INST] Which methods support the evidence found for the RS587776788 SNP? [/INST] Associated methods are: clinical testing, literature only. </s> |
What is the clinical significance of RS587776788 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587776788 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587776788 SNP? | The variation length is 3 base pairs. | <s>[INST] How long is the variation length for RS587776788 SNP? [/INST] The variation length is 3 base pairs. </s> |
What is the origin for RS587776788 SNP? | The origin is germline. | <s>[INST] What is the origin for RS587776788 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS587776788 SNP? | The variation is a Microsatellite. | <s>[INST] What is the type of genetic variation for RS587776788 SNP? [/INST] The variation is a Microsatellite. </s> |
What is the genetic molecular consequence for RS587776788 SNP? | The resulting gene consequence is a inframe_deletion. | <s>[INST] What is the genetic molecular consequence for RS587776788 SNP? [/INST] The resulting gene consequence is a inframe_deletion. </s> |
Which condition is asociated with SNV132309? | 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/RsSNV132309. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV132309. | <s>[INST] Which condition is asociated with SNV132309? [/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/RsSNV132309. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV132309. </s> |
In which chromosome is SNV132309 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV132309 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV132309? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV132309? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV132309, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV132309, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV132309? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV132309? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV132309? | The origin is somatic. | <s>[INST] What is the origin for SNV132309? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for SNV132309? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV132309? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV132309? | The resulting gene consequence is a intron variant. | <s>[INST] What is the genetic molecular consequence for SNV132309? [/INST] The resulting gene consequence is a intron variant. </s> |
Which condition is asociated with RS587778836 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/RsRS587778836 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778836 SNP. | <s>[INST] Which condition is asociated with RS587778836 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/RsRS587778836 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778836 SNP. </s> |
In which chromosome is RS587778836 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778836 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778836 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS587778836 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS587778836 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778836 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587778836 SNP? | The variation length is 4 base pairs. | <s>[INST] How long is the variation length for RS587778836 SNP? [/INST] The variation length is 4 base pairs. </s> |
What is the origin for RS587778836 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS587778836 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS587778836 SNP? | The variation is a Duplication. | <s>[INST] What is the type of genetic variation for RS587778836 SNP? [/INST] The variation is a Duplication. </s> |
What is the genetic molecular consequence for RS587778836 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for RS587778836 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with SNV132312? | 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/RsSNV132312. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV132312. | <s>[INST] Which condition is asociated with SNV132312? [/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/RsSNV132312. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV132312. </s> |
In which chromosome is SNV132312 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV132312 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV132312? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the SNV132312? [/INST] Associated methods are: research. </s> |
What is the clinical significance of SNV132312, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV132312, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV132312? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV132312? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV132312? | The origin is somatic. | <s>[INST] What is the origin for SNV132312? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for SNV132312? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV132312? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV132312? | The resulting gene consequence is a nonsense. | <s>[INST] What is the genetic molecular consequence for SNV132312? [/INST] The resulting gene consequence is a nonsense. </s> |
Which condition is asociated with RS587778837 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/RsRS587778837 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778837 SNP. | <s>[INST] Which condition is asociated with RS587778837 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/RsRS587778837 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778837 SNP. </s> |
In which chromosome is RS587778837 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778837 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778837 SNP? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the RS587778837 SNP? [/INST] Associated methods are: research. </s> |
What is the clinical significance of RS587778837 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778837 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587778837 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS587778837 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS587778837 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS587778837 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS587778837 SNP? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for RS587778837 SNP? [/INST] The variation is a Deletion. </s> |