Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs878853354
rs878853354
A 0.700 GeneticVariation CLINVAR Identity-by-descent-guided mutation analysis and exome sequencing in consanguineous families reveals unusual clinical and molecular findings in retinal dystrophy. 24625443

2014

dbSNP: rs541717028
rs541717028
T 0.700 CausalMutation CLINVAR MERTK arginine-844-cysteine in a patient with severe rod-cone dystrophy: loss of mutant protein function in transfected cells. 15111602

2004

dbSNP: rs527236083
rs527236083
C 0.700 GeneticVariation CLINVAR

dbSNP: rs746238212
rs746238212
G 0.700 GeneticVariation CLINVAR