Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518787
rs1057518787
GPR143
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518802
rs1057518802
SLC19A1 ; COL18A1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518822
rs1057518822
CEP290
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057518836
rs1057518836
NDP ; NDP-AS1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518843
rs1057518843
GALC
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518963
rs1057518963
OPHN1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1085307993
rs1085307993
GABRB2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1114167290
rs1114167290
MYO5A
C 0.700 CausalMutation CLINVAR

dbSNP: rs1114167292
rs1114167292
RUBCN
T 0.700 CausalMutation CLINVAR

dbSNP: rs1135402761
rs1135402761
SYT1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs114925667
rs114925667
UBA5 ; NPHP3-ACAD11
A 0.700 CausalMutation CLINVAR

dbSNP: rs1217391623
rs1217391623
SPG7
T 0.700 CausalMutation CLINVAR

dbSNP: rs121907922
rs121907922
PAX6 ; ELP4
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1276519904
rs1276519904
H3-3A
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1345176461
rs1345176461
IRF2BPL ; LOC107984638
A 0.700 GeneticVariation CLINVAR

dbSNP: rs137852834
rs137852834
CEP290
A 0.700 CausalMutation CLINVAR

dbSNP: rs137853105
rs137853105
MKS1
C 0.700 CausalMutation CLINVAR

dbSNP: rs138504221
rs138504221
SGSH
G 0.700 CausalMutation CLINVAR

dbSNP: rs142285818
rs142285818
RHO
G 0.700 CausalMutation CLINVAR

dbSNP: rs144078282
rs144078282
CLPB
C 0.700 CausalMutation CLINVAR

dbSNP: rs146539065
rs146539065
SEPSECS
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1488635637
rs1488635637
MKS1
G 0.700 CausalMutation CLINVAR

dbSNP: rs150726175
rs150726175
NMNAT1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1553281318
rs1553281318
COQ8A
GA 0.700 GeneticVariation CLINVAR

dbSNP: rs1554110735
rs1554110735
TFAP2A
C 0.700 CausalMutation CLINVAR