Source: INFERRED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894845
rs104894845
G 0.860 CausalMutation CLINVAR

dbSNP: rs104894845
rs104894845
T 0.860 CausalMutation CLINVAR

dbSNP: rs104894848
rs104894848
G 0.820 CausalMutation CLINVAR

dbSNP: rs104894852
rs104894852
C 0.810 CausalMutation CLINVAR

dbSNP: rs28935195
rs28935195
T 0.810 CausalMutation CLINVAR

dbSNP: rs28935494
rs28935494
G 0.810 CausalMutation CLINVAR

dbSNP: rs797044613
rs797044613
G 0.810 CausalMutation CLINVAR

dbSNP: rs104894832
rs104894832
T 0.800 CausalMutation CLINVAR

dbSNP: rs104894836
rs104894836
C 0.800 CausalMutation CLINVAR

dbSNP: rs104894837
rs104894837
A 0.800 CausalMutation CLINVAR

dbSNP: rs104894838
rs104894838
C 0.800 CausalMutation CLINVAR

dbSNP: rs28935196
rs28935196
G 0.800 CausalMutation CLINVAR

dbSNP: rs28935487
rs28935487
A 0.800 CausalMutation CLINVAR

dbSNP: rs28935488
rs28935488
G 0.800 CausalMutation CLINVAR

dbSNP: rs28935489
rs28935489
A 0.800 CausalMutation CLINVAR

dbSNP: rs28935491
rs28935491
T 0.800 CausalMutation CLINVAR

dbSNP: rs28935492
rs28935492
G 0.800 CausalMutation CLINVAR

dbSNP: rs28935495
rs28935495
C 0.800 CausalMutation CLINVAR

dbSNP: rs727504348
rs727504348
T 0.800 CausalMutation CLINVAR

dbSNP: rs869312163
rs869312163
T 0.800 GeneticVariation CLINVAR

dbSNP: rs869312399
rs869312399
C 0.800 CausalMutation CLINVAR

dbSNP: rs104894851
rs104894851
T 0.710 CausalMutation CLINVAR

dbSNP: rs398123226
rs398123226
T 0.710 CausalMutation CLINVAR

dbSNP: rs727503949
rs727503949
A 0.710 CausalMutation CLINVAR

dbSNP: rs104894829
rs104894829
T 0.700 CausalMutation CLINVAR