Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913301
rs121913301
T 0.700 CausalMutation CLINVAR Next-generation sequencing-based method shows increased mutation detection sensitivity in an Indian retinoblastoma cohort. 27582626

2016

dbSNP: rs121913301
rs121913301
T 0.700 GeneticVariation CLINVAR Genetic screening in patients with Retinoblastoma in Israel. 25754945

2015

dbSNP: rs121913301
rs121913301
T 0.700 CausalMutation CLINVAR Targeted next generation sequencing of RB1 gene for the molecular diagnosis of Retinoblastoma. 25928201

2015

dbSNP: rs121913301
rs121913301
T 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014

dbSNP: rs121913301
rs121913301
T 0.700 CausalMutation CLINVAR [Characteristics of RB1 gene mutations in Chinese patients with retinoblastoma]. 24078560

2013

dbSNP: rs121913301
rs121913301
T 0.700 CausalMutation CLINVAR Phenotypic variability of retinocytomas: preregression and postregression growth patterns. 22328814

2012

dbSNP: rs121913301
rs121913301
T 0.700 CausalMutation CLINVAR Mutational analysis of the RB1 gene in Moroccan patients with retinoblastoma. 22219649

2011

dbSNP: rs121913301
rs121913301
T 0.700 CausalMutation CLINVAR Spectrum of germline mutations in the RB1 gene: a study of 232 patients with hereditary and non hereditary retinoblastoma. 7795591

1995