Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913296
rs121913296
RB1
T 0.700 CausalMutation CLINVAR Mutation spectrum of RB1 gene in Korean bilateral retinoblastoma patients using direct sequencing and gene dosage analysis. 22963398

2013
dbSNP: rs121913296
rs121913296
RB1
T 0.700 CausalMutation CLINVAR [Spectrum and frequencies of RB1 gene structural defects in retinoblastoma]. 12173465

2002
dbSNP: rs121913296
rs121913296
RB1
T 0.700 CausalMutation CLINVAR The spectrum of RB1 germ-line mutations in hereditary retinoblastoma. 8651278

1996