Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518776
rs1057518776
DYNC1H1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519465
rs1057519465
HEXA
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057521223
rs1057521223
SCN2A
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1085307993
rs1085307993
GABRB2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1114167292
rs1114167292
RUBCN
T 0.700 CausalMutation CLINVAR

dbSNP: rs1114167295
rs1114167295
MAGED2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1114167296
rs1114167296
TMEM47
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1114167298
rs1114167298
GRM7
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1114167300
rs1114167300
GRM7
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1114167301
rs1114167301
GRM7
A 0.700 GeneticVariation CLINVAR

dbSNP: rs113460156
rs113460156
RYR1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1135402761
rs1135402761
SYT1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs113871094
rs113871094
FBN1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1163944538
rs1163944538
TMEM94
GA 0.700 CausalMutation CLINVAR

dbSNP: rs121907978
rs121907978
HEXA
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1352010373
rs1352010373
TMEM94
C 0.700 CausalMutation CLINVAR

dbSNP: rs137852695
rs137852695
PPT1
A 0.700 CausalMutation CLINVAR

dbSNP: rs137852832
rs137852832
CEP290
A 0.700 CausalMutation CLINVAR

dbSNP: rs137853105
rs137853105
MKS1
C 0.700 CausalMutation CLINVAR

dbSNP: rs139751598
rs139751598
PYCR1
T 0.700 CausalMutation CLINVAR

dbSNP: rs140119177
rs140119177
FAM120AOS
A 0.700 GeneticVariation CLINVAR

dbSNP: rs141760116
rs141760116
SMN1 ; SMN2
G 0.700 CausalMutation CLINVAR

dbSNP: rs143657539
rs143657539
PPT1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1448259271
rs1448259271
IRF2BPL ; LOC107984638
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1488635637
rs1488635637
MKS1
G 0.700 CausalMutation CLINVAR