Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137852673
rs137852673
A 0.700 CausalMutation CLINVAR

dbSNP: rs137852674
rs137852674
C 0.700 CausalMutation CLINVAR

dbSNP: rs137852784
rs137852784
T 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs137853236
rs137853236
T 0.700 CausalMutation CLINVAR

dbSNP: rs141804752
rs141804752
G 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs148311934
rs148311934
T 0.700 CausalMutation CLINVAR

dbSNP: rs1553638903
rs1553638903
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1553638909
rs1553638909
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1553784995
rs1553784995
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1553876668
rs1553876668
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553878211
rs1553878211
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1554901596
rs1554901596
TC 0.700 CausalMutation CLINVAR

dbSNP: rs1554948310
rs1554948310
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555212014
rs1555212014
T 0.700 CausalMutation CLINVAR

dbSNP: rs182349376
rs182349376
T 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs182552223
rs182552223
0.700 GeneticVariation UNIPROT

dbSNP: rs184917682
rs184917682
C 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs193922283
rs193922283
GCK
A 0.700 GeneticVariation CLINVAR

dbSNP: rs193922402
rs193922402
A 0.700 GeneticVariation CLINVAR

dbSNP: rs199474657
rs199474657
ND1 ; ND2 ; TRNL1
G 0.700 CausalMutation CLINVAR

dbSNP: rs267607196
rs267607196
T 0.700 GeneticVariation CLINVAR

dbSNP: rs35449651
rs35449651
0.700 GeneticVariation UNIPROT

dbSNP: rs371977235
rs371977235
T 0.700 CausalMutation CLINVAR

dbSNP: rs387906779
rs387906779
C 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs587777732
rs587777732
T 0.700 CausalMutation CLINVAR