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Which methods support the evidence found for the RS1949505926 SNP? | Associated methods are: clinical testing. | <s>[INST]Which methods support the evidence found for the RS1949505926 SNP?[/INST] Associated methods are: clinical testing.</s> |
What is the clinical significance of RS1949505926 SNP, is it benign or pathogenic? | It is Uncertain significance. | <s>[INST]What is the clinical significance of RS1949505926 SNP, is it benign or pathogenic?[/INST] It is Uncertain significance.</s> |
How long is the variation length for RS1949505926 SNP? | The variation length is 1 base pairs. | <s>[INST]How long is the variation length for RS1949505926 SNP?[/INST] The variation length is 1 base pairs.</s> |
What is the origin for RS1949505926 SNP? | The origin is germline. | <s>[INST]What is the origin for RS1949505926 SNP?[/INST] The origin is germline.</s> |
What is the type of genetic variation for RS1949505926 SNP? | The variation is a single nucleotide variant. | <s>[INST]What is the type of genetic variation for RS1949505926 SNP?[/INST] The variation is a single nucleotide variant.</s> |
What is the genetic molecular consequence for RS1949505926 SNP? | The resulting gene consequence is a missense variant. | <s>[INST]What is the genetic molecular consequence for RS1949505926 SNP?[/INST] The resulting gene consequence is a missense variant.</s> |
Which condition is asociated with RS1952455844 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/RsRS1952455844 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1952455844 SNP. | <s>[INST]Which condition is asociated with RS1952455844 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/RsRS1952455844 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1952455844 SNP.</s> |
In which chromosome is RS1952455844 SNP located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is RS1952455844 SNP located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the RS1952455844 SNP? | Associated methods are: clinical testing. | <s>[INST]Which methods support the evidence found for the RS1952455844 SNP?[/INST] Associated methods are: clinical testing.</s> |
What is the clinical significance of RS1952455844 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST]What is the clinical significance of RS1952455844 SNP, is it benign or pathogenic?[/INST] It is Pathogenic.</s> |
How long is the variation length for RS1952455844 SNP? | The variation length is 2 base pairs. | <s>[INST]How long is the variation length for RS1952455844 SNP?[/INST] The variation length is 2 base pairs.</s> |
What is the origin for RS1952455844 SNP? | The origin is germline. | <s>[INST]What is the origin for RS1952455844 SNP?[/INST] The origin is germline.</s> |
What is the type of genetic variation for RS1952455844 SNP? | The variation is a Microsatellite. | <s>[INST]What is the type of genetic variation for RS1952455844 SNP?[/INST] The variation is a Microsatellite.</s> |
What is the genetic molecular consequence for RS1952455844 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST]What is the genetic molecular consequence for RS1952455844 SNP?[/INST] The resulting gene consequence is a frameshift variant.</s> |
Which condition is asociated with RS1949419453 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/RsRS1949419453 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1949419453 SNP. | <s>[INST]Which condition is asociated with RS1949419453 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/RsRS1949419453 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1949419453 SNP.</s> |
In which chromosome is RS1949419453 SNP located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is RS1949419453 SNP located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the RS1949419453 SNP? | Associated methods are: clinical testing. | <s>[INST]Which methods support the evidence found for the RS1949419453 SNP?[/INST] Associated methods are: clinical testing.</s> |
What is the clinical significance of RS1949419453 SNP, is it benign or pathogenic? | It is Uncertain significance. | <s>[INST]What is the clinical significance of RS1949419453 SNP, is it benign or pathogenic?[/INST] It is Uncertain significance.</s> |
How long is the variation length for RS1949419453 SNP? | The variation length is 1 base pairs. | <s>[INST]How long is the variation length for RS1949419453 SNP?[/INST] The variation length is 1 base pairs.</s> |
What is the origin for RS1949419453 SNP? | The origin is germline. | <s>[INST]What is the origin for RS1949419453 SNP?[/INST] The origin is germline.</s> |
What is the type of genetic variation for RS1949419453 SNP? | The variation is a single nucleotide variant. | <s>[INST]What is the type of genetic variation for RS1949419453 SNP?[/INST] The variation is a single nucleotide variant.</s> |
What is the genetic molecular consequence for RS1949419453 SNP? | The resulting gene consequence is a intron variant. | <s>[INST]What is the genetic molecular consequence for RS1949419453 SNP?[/INST] The resulting gene consequence is a intron variant.</s> |
Which condition is asociated with RS1952053203 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/RsRS1952053203 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1952053203 SNP. | <s>[INST]Which condition is asociated with RS1952053203 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/RsRS1952053203 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1952053203 SNP.</s> |
In which chromosome is RS1952053203 SNP located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is RS1952053203 SNP located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the RS1952053203 SNP? | Associated methods are: clinical testing. | <s>[INST]Which methods support the evidence found for the RS1952053203 SNP?[/INST] Associated methods are: clinical testing.</s> |
What is the clinical significance of RS1952053203 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST]What is the clinical significance of RS1952053203 SNP, is it benign or pathogenic?[/INST] It is Pathogenic.</s> |
How long is the variation length for RS1952053203 SNP? | The variation length is 13 base pairs. | <s>[INST]How long is the variation length for RS1952053203 SNP?[/INST] The variation length is 13 base pairs.</s> |
What is the origin for RS1952053203 SNP? | The origin is germline. | <s>[INST]What is the origin for RS1952053203 SNP?[/INST] The origin is germline.</s> |
What is the type of genetic variation for RS1952053203 SNP? | The variation is a Deletion. | <s>[INST]What is the type of genetic variation for RS1952053203 SNP?[/INST] The variation is a Deletion.</s> |
What is the genetic molecular consequence for RS1952053203 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST]What is the genetic molecular consequence for RS1952053203 SNP?[/INST] The resulting gene consequence is a frameshift variant.</s> |
Which condition is asociated with RS886050268 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/RsRS886050268 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS886050268 SNP. | <s>[INST]Which condition is asociated with RS886050268 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/RsRS886050268 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS886050268 SNP.</s> |
In which chromosome is RS886050268 SNP located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is RS886050268 SNP located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the RS886050268 SNP? | Associated methods are: clinical testing. | <s>[INST]Which methods support the evidence found for the RS886050268 SNP?[/INST] Associated methods are: clinical testing.</s> |
What is the clinical significance of RS886050268 SNP, is it benign or pathogenic? | It is Uncertain significance. | <s>[INST]What is the clinical significance of RS886050268 SNP, is it benign or pathogenic?[/INST] It is Uncertain significance.</s> |
How long is the variation length for RS886050268 SNP? | The variation length is 1 base pairs. | <s>[INST]How long is the variation length for RS886050268 SNP?[/INST] The variation length is 1 base pairs.</s> |
What is the origin for RS886050268 SNP? | The origin is germline. | <s>[INST]What is the origin for RS886050268 SNP?[/INST] The origin is germline.</s> |
What is the type of genetic variation for RS886050268 SNP? | The variation is a single nucleotide variant. | <s>[INST]What is the type of genetic variation for RS886050268 SNP?[/INST] The variation is a single nucleotide variant.</s> |
What is the genetic molecular consequence for RS886050268 SNP? | The resulting gene consequence is a missense variant. | <s>[INST]What is the genetic molecular consequence for RS886050268 SNP?[/INST] The resulting gene consequence is a missense variant.</s> |
Which condition is asociated with RS1952481401 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/RsRS1952481401 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1952481401 SNP. | <s>[INST]Which condition is asociated with RS1952481401 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/RsRS1952481401 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1952481401 SNP.</s> |
In which chromosome is RS1952481401 SNP located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is RS1952481401 SNP located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the RS1952481401 SNP? | Associated methods are: clinical testing. | <s>[INST]Which methods support the evidence found for the RS1952481401 SNP?[/INST] Associated methods are: clinical testing.</s> |
What is the clinical significance of RS1952481401 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST]What is the clinical significance of RS1952481401 SNP, is it benign or pathogenic?[/INST] It is Pathogenic.</s> |
How long is the variation length for RS1952481401 SNP? | The variation length is 1 base pairs. | <s>[INST]How long is the variation length for RS1952481401 SNP?[/INST] The variation length is 1 base pairs.</s> |
What is the origin for RS1952481401 SNP? | The origin is de novo. | <s>[INST]What is the origin for RS1952481401 SNP?[/INST] The origin is de novo.</s> |
What is the type of genetic variation for RS1952481401 SNP? | The variation is a single nucleotide variant. | <s>[INST]What is the type of genetic variation for RS1952481401 SNP?[/INST] The variation is a single nucleotide variant.</s> |
What is the genetic molecular consequence for RS1952481401 SNP? | The resulting gene consequence is a nonsense. | <s>[INST]What is the genetic molecular consequence for RS1952481401 SNP?[/INST] The resulting gene consequence is a nonsense.</s> |
Which condition is asociated with RS1949338513 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/RsRS1949338513 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1949338513 SNP. | <s>[INST]Which condition is asociated with RS1949338513 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/RsRS1949338513 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1949338513 SNP.</s> |
In which chromosome is RS1949338513 SNP located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is RS1949338513 SNP located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the RS1949338513 SNP? | Associated methods are: clinical testing. | <s>[INST]Which methods support the evidence found for the RS1949338513 SNP?[/INST] Associated methods are: clinical testing.</s> |
What is the clinical significance of RS1949338513 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST]What is the clinical significance of RS1949338513 SNP, is it benign or pathogenic?[/INST] It is Pathogenic.</s> |
How long is the variation length for RS1949338513 SNP? | The variation length is 1 base pairs. | <s>[INST]How long is the variation length for RS1949338513 SNP?[/INST] The variation length is 1 base pairs.</s> |
What is the origin for RS1949338513 SNP? | The origin is germline. | <s>[INST]What is the origin for RS1949338513 SNP?[/INST] The origin is germline.</s> |
What is the type of genetic variation for RS1949338513 SNP? | The variation is a Deletion. | <s>[INST]What is the type of genetic variation for RS1949338513 SNP?[/INST] The variation is a Deletion.</s> |
What is the genetic molecular consequence for RS1949338513 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST]What is the genetic molecular consequence for RS1949338513 SNP?[/INST] The resulting gene consequence is a frameshift variant.</s> |
Which condition is asociated with RS1949359603 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/RsRS1949359603 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1949359603 SNP. | <s>[INST]Which condition is asociated with RS1949359603 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/RsRS1949359603 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1949359603 SNP.</s> |
In which chromosome is RS1949359603 SNP located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is RS1949359603 SNP located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the RS1949359603 SNP? | Associated methods are: research. | <s>[INST]Which methods support the evidence found for the RS1949359603 SNP?[/INST] Associated methods are: research.</s> |
What is the clinical significance of RS1949359603 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST]What is the clinical significance of RS1949359603 SNP, is it benign or pathogenic?[/INST] It is Pathogenic.</s> |
How long is the variation length for RS1949359603 SNP? | The variation length is 1 base pairs. | <s>[INST]How long is the variation length for RS1949359603 SNP?[/INST] The variation length is 1 base pairs.</s> |
What is the origin for RS1949359603 SNP? | The origin is somatic. | <s>[INST]What is the origin for RS1949359603 SNP?[/INST] The origin is somatic.</s> |
What is the type of genetic variation for RS1949359603 SNP? | The variation is a single nucleotide variant. | <s>[INST]What is the type of genetic variation for RS1949359603 SNP?[/INST] The variation is a single nucleotide variant.</s> |
What is the genetic molecular consequence for RS1949359603 SNP? | The resulting gene consequence is a nonsense. | <s>[INST]What is the genetic molecular consequence for RS1949359603 SNP?[/INST] The resulting gene consequence is a nonsense.</s> |
Which condition is asociated with RS1949384403 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/RsRS1949384403 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1949384403 SNP. | <s>[INST]Which condition is asociated with RS1949384403 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/RsRS1949384403 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1949384403 SNP.</s> |
In which chromosome is RS1949384403 SNP located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is RS1949384403 SNP located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the RS1949384403 SNP? | Associated methods are: research. | <s>[INST]Which methods support the evidence found for the RS1949384403 SNP?[/INST] Associated methods are: research.</s> |
What is the clinical significance of RS1949384403 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST]What is the clinical significance of RS1949384403 SNP, is it benign or pathogenic?[/INST] It is Pathogenic.</s> |
How long is the variation length for RS1949384403 SNP? | The variation length is 4 base pairs. | <s>[INST]How long is the variation length for RS1949384403 SNP?[/INST] The variation length is 4 base pairs.</s> |
What is the origin for RS1949384403 SNP? | The origin is somatic. | <s>[INST]What is the origin for RS1949384403 SNP?[/INST] The origin is somatic.</s> |
What is the type of genetic variation for RS1949384403 SNP? | The variation is a Duplication. | <s>[INST]What is the type of genetic variation for RS1949384403 SNP?[/INST] The variation is a Duplication.</s> |
What is the genetic molecular consequence for RS1949384403 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST]What is the genetic molecular consequence for RS1949384403 SNP?[/INST] The resulting gene consequence is a frameshift variant.</s> |
Which condition is asociated with SNV1048360? | 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/RsSNV1048360. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1048360. | <s>[INST]Which condition is asociated with SNV1048360?[/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/RsSNV1048360. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1048360.</s> |
In which chromosome is SNV1048360 located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is SNV1048360 located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the SNV1048360? | Associated methods are: clinical testing. | <s>[INST]Which methods support the evidence found for the SNV1048360?[/INST] Associated methods are: clinical testing.</s> |
What is the clinical significance of SNV1048360, is it benign or pathogenic? | It is Uncertain significance. | <s>[INST]What is the clinical significance of SNV1048360, is it benign or pathogenic?[/INST] It is Uncertain significance.</s> |
How long is the variation length for SNV1048360? | The variation length is 1 base pairs. | <s>[INST]How long is the variation length for SNV1048360?[/INST] The variation length is 1 base pairs.</s> |
What is the origin for SNV1048360? | The origin is germline. | <s>[INST]What is the origin for SNV1048360?[/INST] The origin is germline.</s> |
What is the type of genetic variation for SNV1048360? | The variation is a single nucleotide variant. | <s>[INST]What is the type of genetic variation for SNV1048360?[/INST] The variation is a single nucleotide variant.</s> |
What is the genetic molecular consequence for SNV1048360? | The resulting gene consequence is a missense variant. | <s>[INST]What is the genetic molecular consequence for SNV1048360?[/INST] The resulting gene consequence is a missense variant.</s> |
Which condition is asociated with DEL1052625? | 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/RsDEL1052625. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL1052625. | <s>[INST]Which condition is asociated with DEL1052625?[/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/RsDEL1052625. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL1052625.</s> |
In which chromosome is DEL1052625 located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is DEL1052625 located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the DEL1052625? | Associated methods are: research. | <s>[INST]Which methods support the evidence found for the DEL1052625?[/INST] Associated methods are: research.</s> |
What is the clinical significance of DEL1052625, is it benign or pathogenic? | It is Pathogenic. | <s>[INST]What is the clinical significance of DEL1052625, is it benign or pathogenic?[/INST] It is Pathogenic.</s> |
How long is the variation length for DEL1052625? | The variation length is 7 base pairs. | <s>[INST]How long is the variation length for DEL1052625?[/INST] The variation length is 7 base pairs.</s> |
What is the origin for DEL1052625? | The origin is germline. | <s>[INST]What is the origin for DEL1052625?[/INST] The origin is germline.</s> |
What is the type of genetic variation for DEL1052625? | The variation is a Deletion. | <s>[INST]What is the type of genetic variation for DEL1052625?[/INST] The variation is a Deletion.</s> |
What is the genetic molecular consequence for DEL1052625? | The resulting gene consequence is a splice acceptor variant. | <s>[INST]What is the genetic molecular consequence for DEL1052625?[/INST] The resulting gene consequence is a splice acceptor variant.</s> |
Which condition is asociated with SNV1052626? | 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/RsSNV1052626. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1052626. | <s>[INST]Which condition is asociated with SNV1052626?[/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/RsSNV1052626. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1052626.</s> |
In which chromosome is SNV1052626 located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is SNV1052626 located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the SNV1052626? | Associated methods are: research. | <s>[INST]Which methods support the evidence found for the SNV1052626?[/INST] Associated methods are: research.</s> |
What is the clinical significance of SNV1052626, is it benign or pathogenic? | It is Likely pathogenic. | <s>[INST]What is the clinical significance of SNV1052626, is it benign or pathogenic?[/INST] It is Likely pathogenic.</s> |
How long is the variation length for SNV1052626? | The variation length is 1 base pairs. | <s>[INST]How long is the variation length for SNV1052626?[/INST] The variation length is 1 base pairs.</s> |
What is the origin for SNV1052626? | The origin is germline. | <s>[INST]What is the origin for SNV1052626?[/INST] The origin is germline.</s> |
What is the type of genetic variation for SNV1052626? | The variation is a single nucleotide variant. | <s>[INST]What is the type of genetic variation for SNV1052626?[/INST] The variation is a single nucleotide variant.</s> |
What is the genetic molecular consequence for SNV1052626? | The resulting gene consequence is a missense variant. | <s>[INST]What is the genetic molecular consequence for SNV1052626?[/INST] The resulting gene consequence is a missense variant.</s> |
Which condition is asociated with SNV1052627? | 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/RsSNV1052627. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1052627. | <s>[INST]Which condition is asociated with SNV1052627?[/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/RsSNV1052627. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1052627.</s> |
In which chromosome is SNV1052627 located? | It is located in the chromosome 13. | <s>[INST]In which chromosome is SNV1052627 located?[/INST] It is located in the chromosome 13.</s> |
Which methods support the evidence found for the SNV1052627? | Associated methods are: research. | <s>[INST]Which methods support the evidence found for the SNV1052627?[/INST] Associated methods are: research.</s> |
What is the clinical significance of SNV1052627, is it benign or pathogenic? | It is Uncertain significance. | <s>[INST]What is the clinical significance of SNV1052627, is it benign or pathogenic?[/INST] It is Uncertain significance.</s> |
How long is the variation length for SNV1052627? | The variation length is 1 base pairs. | <s>[INST]How long is the variation length for SNV1052627?[/INST] The variation length is 1 base pairs.</s> |
What is the origin for SNV1052627? | The origin is germline. | <s>[INST]What is the origin for SNV1052627?[/INST] The origin is germline.</s> |