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What is the genetic molecular consequence for RS587778837 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for RS587778837 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with RS587778851 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/RsRS587778851 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778851 SNP. | <s>[INST] Which condition is asociated with RS587778851 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/RsRS587778851 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778851 SNP. </s> |
In which chromosome is RS587778851 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778851 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778851 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS587778851 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS587778851 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778851 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587778851 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS587778851 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS587778851 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS587778851 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS587778851 SNP? | The variation is a Duplication. | <s>[INST] What is the type of genetic variation for RS587778851 SNP? [/INST] The variation is a Duplication. </s> |
What is the genetic molecular consequence for RS587778851 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for RS587778851 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with RS587778825 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/RsRS587778825 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778825 SNP. | <s>[INST] Which condition is asociated with RS587778825 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/RsRS587778825 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778825 SNP. </s> |
In which chromosome is RS587778825 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778825 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778825 SNP? | Associated methods are: research, clinical testing. | <s>[INST] Which methods support the evidence found for the RS587778825 SNP? [/INST] Associated methods are: research, clinical testing. </s> |
What is the clinical significance of RS587778825 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778825 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587778825 SNP? | The variation length is 2 base pairs. | <s>[INST] How long is the variation length for RS587778825 SNP? [/INST] The variation length is 2 base pairs. </s> |
What is the origin for RS587778825 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS587778825 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS587778825 SNP? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for RS587778825 SNP? [/INST] The variation is a Deletion. </s> |
What is the genetic molecular consequence for RS587778825 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for RS587778825 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with RS587778841 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/RsRS587778841 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778841 SNP. | <s>[INST] Which condition is asociated with RS587778841 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/RsRS587778841 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778841 SNP. </s> |
In which chromosome is RS587778841 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778841 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778841 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS587778841 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS587778841 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778841 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587778841 SNP? | The variation length is 4 base pairs. | <s>[INST] How long is the variation length for RS587778841 SNP? [/INST] The variation length is 4 base pairs. </s> |
What is the origin for RS587778841 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS587778841 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS587778841 SNP? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for RS587778841 SNP? [/INST] The variation is a Deletion. </s> |
What is the genetic molecular consequence for RS587778841 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for RS587778841 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with RS587778854 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/RsRS587778854 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778854 SNP. | <s>[INST] Which condition is asociated with RS587778854 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/RsRS587778854 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778854 SNP. </s> |
In which chromosome is RS587778854 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778854 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778854 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS587778854 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS587778854 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778854 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587778854 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS587778854 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS587778854 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS587778854 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS587778854 SNP? | The variation is a Duplication. | <s>[INST] What is the type of genetic variation for RS587778854 SNP? [/INST] The variation is a Duplication. </s> |
What is the genetic molecular consequence for RS587778854 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for RS587778854 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with RS886037649 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/RsRS886037649 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS886037649 SNP. | <s>[INST] Which condition is asociated with RS886037649 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/RsRS886037649 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS886037649 SNP. </s> |
In which chromosome is RS886037649 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS886037649 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS886037649 SNP? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the RS886037649 SNP? [/INST] Associated methods are: research. </s> |
What is the clinical significance of RS886037649 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS886037649 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS886037649 SNP? | The variation length is 3 base pairs. | <s>[INST] How long is the variation length for RS886037649 SNP? [/INST] The variation length is 3 base pairs. </s> |
What is the origin for RS886037649 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS886037649 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS886037649 SNP? | The variation is a Indel. | <s>[INST] What is the type of genetic variation for RS886037649 SNP? [/INST] The variation is a Indel. </s> |
What is the genetic molecular consequence for RS886037649 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for RS886037649 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with RS587778827 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/RsRS587778827 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778827 SNP. | <s>[INST] Which condition is asociated with RS587778827 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/RsRS587778827 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778827 SNP. </s> |
In which chromosome is RS587778827 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778827 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778827 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS587778827 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS587778827 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778827 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587778827 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS587778827 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS587778827 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS587778827 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS587778827 SNP? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for RS587778827 SNP? [/INST] The variation is a Deletion. </s> |
What is the genetic molecular consequence for RS587778827 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for RS587778827 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with RS587778828 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/RsRS587778828 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778828 SNP. | <s>[INST] Which condition is asociated with RS587778828 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/RsRS587778828 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778828 SNP. </s> |
In which chromosome is RS587778828 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778828 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778828 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS587778828 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS587778828 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778828 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587778828 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS587778828 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS587778828 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS587778828 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS587778828 SNP? | The variation is a Duplication. | <s>[INST] What is the type of genetic variation for RS587778828 SNP? [/INST] The variation is a Duplication. </s> |
What is the genetic molecular consequence for RS587778828 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for RS587778828 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with RS587778844 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/RsRS587778844 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778844 SNP. | <s>[INST] Which condition is asociated with RS587778844 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/RsRS587778844 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778844 SNP. </s> |
In which chromosome is RS587778844 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778844 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778844 SNP? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the RS587778844 SNP? [/INST] Associated methods are: research. </s> |
What is the clinical significance of RS587778844 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778844 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587778844 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS587778844 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS587778844 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS587778844 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS587778844 SNP? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for RS587778844 SNP? [/INST] The variation is a Deletion. </s> |
What is the genetic molecular consequence for RS587778844 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for RS587778844 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with RS587778829 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/RsRS587778829 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778829 SNP. | <s>[INST] Which condition is asociated with RS587778829 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/RsRS587778829 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778829 SNP. </s> |
In which chromosome is RS587778829 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778829 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778829 SNP? | Associated methods are: research, clinical testing. | <s>[INST] Which methods support the evidence found for the RS587778829 SNP? [/INST] Associated methods are: research, clinical testing. </s> |
What is the clinical significance of RS587778829 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778829 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587778829 SNP? | The variation length is 2 base pairs. | <s>[INST] How long is the variation length for RS587778829 SNP? [/INST] The variation length is 2 base pairs. </s> |
What is the origin for RS587778829 SNP? | The origin is germline. | <s>[INST] What is the origin for RS587778829 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS587778829 SNP? | The variation is a Microsatellite. | <s>[INST] What is the type of genetic variation for RS587778829 SNP? [/INST] The variation is a Microsatellite. </s> |
What is the genetic molecular consequence for RS587778829 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for RS587778829 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with RS587778830 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/RsRS587778830 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778830 SNP. | <s>[INST] Which condition is asociated with RS587778830 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/RsRS587778830 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778830 SNP. </s> |
In which chromosome is RS587778830 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778830 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778830 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS587778830 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS587778830 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778830 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587778830 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS587778830 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS587778830 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS587778830 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS587778830 SNP? | The variation is a Duplication. | <s>[INST] What is the type of genetic variation for RS587778830 SNP? [/INST] The variation is a Duplication. </s> |
What is the genetic molecular consequence for RS587778830 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for RS587778830 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with RS587778832 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/RsRS587778832 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778832 SNP. | <s>[INST] Which condition is asociated with RS587778832 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/RsRS587778832 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778832 SNP. </s> |
In which chromosome is RS587778832 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778832 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778832 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS587778832 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS587778832 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778832 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587778832 SNP? | The variation length is 2 base pairs. | <s>[INST] How long is the variation length for RS587778832 SNP? [/INST] The variation length is 2 base pairs. </s> |
What is the origin for RS587778832 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS587778832 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS587778832 SNP? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for RS587778832 SNP? [/INST] The variation is a Deletion. </s> |
What is the genetic molecular consequence for RS587778832 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for RS587778832 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with RS587778840 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/RsRS587778840 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778840 SNP. | <s>[INST] Which condition is asociated with RS587778840 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/RsRS587778840 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778840 SNP. </s> |
In which chromosome is RS587778840 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778840 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778840 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS587778840 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS587778840 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778840 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587778840 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS587778840 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS587778840 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS587778840 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS587778840 SNP? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for RS587778840 SNP? [/INST] The variation is a Deletion. </s> |
What is the genetic molecular consequence for RS587778840 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for RS587778840 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with RS587778862 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/RsRS587778862 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778862 SNP. | <s>[INST] Which condition is asociated with RS587778862 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/RsRS587778862 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778862 SNP. </s> |
In which chromosome is RS587778862 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778862 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778862 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS587778862 SNP? [/INST] Associated methods are: clinical testing. </s> |