Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1569484091
rs1569484091
ATP6 ; ATP8 ; COX1 ; COX2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1569484096
rs1569484096
ATP6 ; ATP8 ; COX1 ; COX2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1569484098
rs1569484098
ATP6 ; ATP8 ; COX1 ; COX2
TCAC 0.700 CausalMutation CLINVAR

dbSNP: rs1569484100
rs1569484100
ATP6 ; ATP8 ; COX1 ; COX2
G 0.700 CausalMutation CLINVAR

dbSNP: rs1569484107
rs1569484107
ATP6 ; ATP8 ; COX1 ; COX2
TTGG 0.700 CausalMutation CLINVAR

dbSNP: rs1569484108
rs1569484108
ATP6 ; ATP8 ; COX1 ; COX2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1569484169
rs1569484169
ATP6 ; ATP8 ; COX1 ; COX2 ; COX3
TGTC 0.700 CausalMutation CLINVAR

dbSNP: rs1569484177
rs1569484177
ATP6 ; ATP8 ; COX1 ; COX2 ; COX3
GCTC 0.700 CausalMutation CLINVAR

dbSNP: rs1569484178
rs1569484178
ATP6 ; ATP8 ; COX1 ; COX2 ; COX3
GCCC 0.700 CausalMutation CLINVAR

dbSNP: rs1569484221
rs1569484221
ATP6 ; ATP8 ; COX2 ; COX3 ; ND3 ; ND4L
CCCA 0.700 CausalMutation CLINVAR