Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80338950
rs80338950
GJB2
CUI: C3887873
Disease: Hearing Loss
Hearing Loss 		G 0.700 CausalMutation CLINVAR

dbSNP: rs80338950
rs80338950
GJB2
CUI: C3887873
Disease: Hearing Loss
Hearing Loss 		T 0.700 CausalMutation CLINVAR