Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs767011440
rs767011440
0.700 GeneticVariation UNIPROT Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics. 27854360

2017

dbSNP: rs767011440
rs767011440
0.700 GeneticVariation UNIPROT ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing. 25356965

2015

dbSNP: rs767011440
rs767011440
0.700 GeneticVariation UNIPROT A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment. 25394175

2015

dbSNP: rs767011440
rs767011440
0.700 GeneticVariation UNIPROT American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers. 24493721

2014

dbSNP: rs767011440
rs767011440
0.700 GeneticVariation UNIPROT ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. 23788249

2013

dbSNP: rs767011440
rs767011440
0.700 GeneticVariation UNIPROT Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors. 15604628

2004

dbSNP: rs767011440
rs767011440
0.700 GeneticVariation UNIPROT Identification of four novel RB1 germline mutations in Korean retinoblastoma patients. 11524739

2001

dbSNP: rs767011440
rs767011440
0.700 GeneticVariation UNIPROT RB1 gene mutations in peripheral blood DNA of patients with isolated unilateral retinoblastoma. 9973307

1999

dbSNP: rs767011440
rs767011440
0.700 GeneticVariation UNIPROT Twelve novel RB1 gene mutations in patients with hereditary retinoblastoma. Mutations in brief no. 206. Online. 10671068

1998

dbSNP: rs767011440
rs767011440
0.700 GeneticVariation UNIPROT Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma. 9311732

1997

dbSNP: rs767011440
rs767011440
0.700 GeneticVariation UNIPROT Genetics of retinoblastoma: a study. 9140452

1997

dbSNP: rs767011440
rs767011440
0.700 GeneticVariation UNIPROT Mutational scanning of large genes by extensive PCR multiplexing and two-dimensional electrophoresis: application to the RB1 gene. 8776589

1996

dbSNP: rs767011440
rs767011440
0.700 GeneticVariation UNIPROT Spectrum of germline mutations in the RB1 gene: a study of 232 patients with hereditary and non hereditary retinoblastoma. 7795591

1995

dbSNP: rs767011440
rs767011440
0.700 GeneticVariation UNIPROT Germline mutations in the RB1 gene in patients with hereditary retinoblastoma. 8605116

1995

dbSNP: rs767011440
rs767011440
0.700 GeneticVariation UNIPROT Frequent constitutional C to T mutations in CGA-arginine codons in the RB1 gene produce premature stop codons in patients with bilateral (hereditary) retinoblastoma. 7704558

1994

dbSNP: rs767011440
rs767011440
0.700 GeneticVariation UNIPROT Distinct RB1 gene mutations with low penetrance in hereditary retinoblastoma. 7927327

1994

dbSNP: rs767011440
rs767011440
0.700 GeneticVariation UNIPROT Molecular mechanisms of oncogenic mutations in tumors from patients with bilateral and unilateral retinoblastoma. 8346255

1993

dbSNP: rs767011440
rs767011440
0.700 GeneticVariation UNIPROT Oncogenic point mutations in exon 20 of the RB1 gene in families showing incomplete penetrance and mild expression of the retinoblastoma phenotype. 1352883

1992

dbSNP: rs767011440
rs767011440
0.700 GeneticVariation UNIPROT Oncogenic point mutations in the human retinoblastoma gene: their application to genetic counseling. 2594029

1989