Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs29001566
rs29001566
RHO
G 0.740 GeneticVariation CLINVAR

dbSNP: rs104893772
rs104893772
RHO
A 0.710 GeneticVariation CLINVAR

dbSNP: rs104893781
rs104893781
RHO
T 0.710 GeneticVariation CLINVAR

dbSNP: rs104893786
rs104893786
RHO
G 0.710 CausalMutation CLINVAR

dbSNP: rs112029032
rs112029032
A 0.710 CausalMutation CLINVAR

dbSNP: rs200946638
rs200946638
RHO
A 0.710 CausalMutation CLINVAR

dbSNP: rs267606691
rs267606691
A 0.710 CausalMutation CLINVAR

dbSNP: rs527236067
rs527236067
PHF3 ; EYS
T 0.710 CausalMutation CLINVAR

dbSNP: rs527236076
rs527236076
PHF3 ; EYS
T 0.710 GeneticVariation CLINVAR

dbSNP: rs753942596
rs753942596
A 0.710 GeneticVariation CLINVAR

dbSNP: rs753942596
rs753942596
A 0.710 CausalMutation CLINVAR

dbSNP: rs80338904
rs80338904
C 0.710 GeneticVariation CLINVAR

dbSNP: rs1035024403
rs1035024403
T 0.700 GeneticVariation CLINVAR

dbSNP: rs104893794
rs104893794
RHO
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518949
rs1057518949
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1060499783
rs1060499783
A 0.700 CausalMutation CLINVAR

dbSNP: rs1064793013
rs1064793013
T 0.700 CausalMutation CLINVAR

dbSNP: rs112822256
rs112822256
EYS
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1168101857
rs1168101857
PHF3 ; EYS
C 0.700 CausalMutation CLINVAR

dbSNP: rs1172628170
rs1172628170
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1177198729
rs1177198729
A 0.700 CausalMutation CLINVAR

dbSNP: rs1178184685
rs1178184685
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1182983579
rs1182983579
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1207247951
rs1207247951
T 0.700 CausalMutation CLINVAR

dbSNP: rs121434241
rs121434241
T 0.700 CausalMutation CLINVAR