Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs867410737
rs867410737
ATP5F1D
T 0.700 CausalMutation CLINVAR Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder. 29478781

2018
dbSNP: rs114303883
rs114303883
ABCC6
A 0.700 CausalMutation CLINVAR

dbSNP: rs1481200467
rs1481200467
ABCC6
C 0.700 CausalMutation CLINVAR

dbSNP: rs1553603732
rs1553603732
DES
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555512158
rs1555512158
ABCC6
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555513085
rs1555513085
ABCC6
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555514089
rs1555514089
ABCC6
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555514467
rs1555514467
ABCC6
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555520991
rs1555520991
ABCC6 ; LOC105371100
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555735545
rs1555735545
STRN4 ; FKRP
A 0.700 CausalMutation CLINVAR

dbSNP: rs2856597
rs2856597
ABCC6
T 0.700 CausalMutation CLINVAR

dbSNP: rs28937900
rs28937900
FKRP
A 0.700 CausalMutation CLINVAR

dbSNP: rs28939702
rs28939702
ABCC6
A 0.700 CausalMutation CLINVAR

dbSNP: rs60791294
rs60791294
ABCC6
T 0.700 CausalMutation CLINVAR

dbSNP: rs63749794
rs63749794
ABCC6
A 0.700 CausalMutation CLINVAR

dbSNP: rs63749796
rs63749796
ABCC6
G 0.700 CausalMutation CLINVAR

dbSNP: rs63749856
rs63749856
ABCC6
T 0.700 CausalMutation CLINVAR

dbSNP: rs63750410
rs63750410
ABCC6
G 0.700 CausalMutation CLINVAR

dbSNP: rs63750428
rs63750428
ABCC6
A 0.700 CausalMutation CLINVAR

dbSNP: rs63750459
rs63750459
ABCC6
A 0.700 CausalMutation CLINVAR

dbSNP: rs63750622
rs63750622
ABCC6
T 0.700 CausalMutation CLINVAR

dbSNP: rs63750759
rs63750759
ABCC6
A 0.700 CausalMutation CLINVAR

dbSNP: rs63751001
rs63751001
ABCC6
T 0.700 CausalMutation CLINVAR

dbSNP: rs63751111
rs63751111
ABCC6
G 0.700 CausalMutation CLINVAR

dbSNP: rs63751241
rs63751241
ABCC6
T 0.700 CausalMutation CLINVAR