Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs146170087
rs146170087
C19orf12
C 0.710 CausalMutation CLINVAR

dbSNP: rs1057518942
rs1057518942
NPC1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1085307993
rs1085307993
GABRB2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1114167290
rs1114167290
MYO5A
C 0.700 CausalMutation CLINVAR

dbSNP: rs1131692231
rs1131692231
CYFIP2
T 0.700 CausalMutation CLINVAR

dbSNP: rs113371321
rs113371321
NPC1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1135401746
rs1135401746
GNB1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs113994063
rs113994063
EIF2B5
T 0.700 CausalMutation CLINVAR

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

dbSNP: rs121917762
rs121917762
TH
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1247665387
rs1247665387
FA2H
A 0.700 GeneticVariation CLINVAR

dbSNP: rs137852968
rs137852968
PANK2 ; MIR103A2
T 0.700 CausalMutation CLINVAR

dbSNP: rs150321966
rs150321966
ECHS1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1553547838
rs1553547838
SATB2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1553621496
rs1553621496
UNC80
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1553770577
rs1553770577
UBA5 ; NPHP3-ACAD11
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1554208945
rs1554208945
ZNF292
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1554317002
rs1554317002
CDK13 ; LOC112267983
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554389088
rs1554389088
CAMK2B
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1554504663
rs1554504663
RHOBTB2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1554504684
rs1554504684
RHOBTB2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555507479
rs1555507479
GNAO1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555582065
rs1555582065
UBTF ; LOC101926967
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555731819
rs1555731819
KMT2B
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1561515242
rs1561515242
CAMK4
A 0.700 GeneticVariation CLINVAR