Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28939668
rs28939668
T 0.830 CausalMutation CLINVAR

dbSNP: rs115099192
rs115099192
A 0.810 CausalMutation CLINVAR

dbSNP: rs115099192
rs115099192
0.810 GeneticVariation UNIPROT

dbSNP: rs28936670
rs28936670
A 0.810 CausalMutation CLINVAR

dbSNP: rs28936670
rs28936670
0.810 GeneticVariation UNIPROT

dbSNP: rs104893905
rs104893905
A 0.800 CausalMutation CLINVAR

dbSNP: rs121434424
rs121434424
T 0.800 CausalMutation CLINVAR

dbSNP: rs187043152
rs187043152
A 0.800 CausalMutation CLINVAR

dbSNP: rs187043152
rs187043152
0.800 GeneticVariation UNIPROT

dbSNP: rs387906769
rs387906769
T 0.710 CausalMutation CLINVAR

dbSNP: rs56208331
rs56208331
A 0.710 CausalMutation CLINVAR

dbSNP: rs121918351
rs121918351
T 0.700 CausalMutation CLINVAR

dbSNP: rs1445910672
rs1445910672
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1554034812
rs1554034812
A 0.700 CausalMutation CLINVAR

dbSNP: rs1556165162
rs1556165162
T 0.700 CausalMutation CLINVAR

dbSNP: rs1569484042
rs1569484042
COX1 ; COX2 ; ND2
C 0.700 CausalMutation CLINVAR

dbSNP: rs1569484120
rs1569484120
ATP6 ; ATP8 ; COX1 ; COX2
CGGG 0.700 GeneticVariation CLINVAR

dbSNP: rs1569484122
rs1569484122
ATP6 ; ATP8 ; COX1 ; COX2
G 0.700 CausalMutation CLINVAR

dbSNP: rs1569484124
rs1569484124
ATP6 ; ATP8 ; COX1 ; COX2
G 0.700 CausalMutation CLINVAR

dbSNP: rs1569484126
rs1569484126
ATP6 ; ATP8 ; COX1 ; COX2
C 0.700 CausalMutation CLINVAR

dbSNP: rs1569484164
rs1569484164
ATP6 ; ATP8 ; COX1 ; COX2 ; COX3
G 0.700 CausalMutation CLINVAR

dbSNP: rs1569484288
rs1569484288
ATP6 ; COX3 ; ND3 ; ND4 ; ND4L
TATC 0.700 CausalMutation CLINVAR

dbSNP: rs1569484299
rs1569484299
ATP6 ; COX3 ; ND3 ; ND4 ; ND4L
GCCC 0.700 CausalMutation CLINVAR

dbSNP: rs1569484301
rs1569484301
ATP6 ; COX3 ; ND3 ; ND4 ; ND4L
CTTT 0.700 CausalMutation CLINVAR

dbSNP: rs201442000
rs201442000
0.700 GeneticVariation UNIPROT