Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28897690
rs28897690
0.700 GeneticVariation UNIPROT

dbSNP: rs387906563
rs387906563
GCCACATGGCT 0.700 CausalMutation CLINVAR

dbSNP: rs397507218
rs397507218
G 0.700 CausalMutation CLINVAR

dbSNP: rs397509067
rs397509067
G 0.700 CausalMutation CLINVAR

dbSNP: rs397509312
rs397509312
C 0.700 CausalMutation CLINVAR

dbSNP: rs41293465
rs41293465
A 0.700 CausalMutation CLINVAR

dbSNP: rs431825390
rs431825390
CCA 0.700 CausalMutation CLINVAR

dbSNP: rs587781258
rs587781258
C 0.700 CausalMutation CLINVAR

dbSNP: rs62625307
rs62625307
A 0.700 CausalMutation CLINVAR

dbSNP: rs62625308
rs62625308
A 0.700 CausalMutation CLINVAR

dbSNP: rs730881439
rs730881439
A 0.700 CausalMutation CLINVAR

dbSNP: rs730881473
rs730881473
A 0.700 CausalMutation CLINVAR

dbSNP: rs730882166
rs730882166
0.700 GeneticVariation UNIPROT

dbSNP: rs80356880
rs80356880
T 0.700 CausalMutation CLINVAR

dbSNP: rs80356885
rs80356885
T 0.700 CausalMutation CLINVAR

dbSNP: rs80356935
rs80356935
T 0.700 CausalMutation CLINVAR

dbSNP: rs80356937
rs80356937
0.700 GeneticVariation UNIPROT

dbSNP: rs80356938
rs80356938
0.700 GeneticVariation UNIPROT

dbSNP: rs80356953
rs80356953
T 0.700 CausalMutation CLINVAR

dbSNP: rs80356962
rs80356962
T 0.700 CausalMutation CLINVAR

dbSNP: rs80356978
rs80356978
A 0.700 CausalMutation CLINVAR

dbSNP: rs80356991
rs80356991
A 0.700 CausalMutation CLINVAR

dbSNP: rs80357001
rs80357001
0.700 GeneticVariation UNIPROT

dbSNP: rs80357015
rs80357015
0.700 GeneticVariation UNIPROT

dbSNP: rs80357082
rs80357082
A 0.700 CausalMutation CLINVAR