Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs62636275
rs62636275
A 0.710 CausalMutation CLINVAR

dbSNP: rs62645752
rs62645752
T 0.700 GeneticVariation CLINVAR Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy. 30718709

2019

dbSNP: rs114342808
rs114342808
T 0.700 CausalMutation CLINVAR

dbSNP: rs150412614
rs150412614
T 0.700 CausalMutation CLINVAR

dbSNP: rs1553261468
rs1553261468
TC 0.700 GeneticVariation CLINVAR

dbSNP: rs281865175
rs281865175
A 0.700 CausalMutation CLINVAR

dbSNP: rs62636271
rs62636271
C 0.700 GeneticVariation CLINVAR

dbSNP: rs62645747
rs62645747
C 0.700 CausalMutation CLINVAR

dbSNP: rs62645748
rs62645748
A 0.700 CausalMutation CLINVAR