Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121917762
rs121917762
TH
T 0.800 CausalMutation CLINVAR

dbSNP: rs121917765
rs121917765
TH
A 0.800 CausalMutation CLINVAR

dbSNP: rs28934581
rs28934581
TH
G 0.800 CausalMutation CLINVAR

dbSNP: rs45471299
rs45471299
TH
A 0.800 CausalMutation CLINVAR

dbSNP: rs45471299
rs45471299
TH
0.800 GeneticVariation UNIPROT

dbSNP: rs104894434
rs104894434
GCH1
G 0.700 CausalMutation CLINVAR

dbSNP: rs104894435
rs104894435
GCH1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057516491
rs1057516491
TH
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057516712
rs1057516712
TH
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057516716
rs1057516716
TH ; MIR4686
CG 0.700 GeneticVariation CLINVAR

dbSNP: rs1057516736
rs1057516736
TH
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057516819
rs1057516819
TH
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057516874
rs1057516874
TH
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517003
rs1057517003
TH
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517162
rs1057517162
TH
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1264884607
rs1264884607
TH
0.700 GeneticVariation UNIPROT

dbSNP: rs1266265578
rs1266265578
TH
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1273610334
rs1273610334
TH
0.700 GeneticVariation UNIPROT

dbSNP: rs137852633
rs137852633
GCH1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1554922441
rs1554922441
TH
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554922593
rs1554922593
TH
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1554923004
rs1554923004
TH
GC 0.700 GeneticVariation CLINVAR

dbSNP: rs1554923121
rs1554923121
TH
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1554923305
rs1554923305
TH
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1554923317
rs1554923317
TH
T 0.700 GeneticVariation CLINVAR