rs80338948, GJB2

N. diseases: 12
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hearing Loss
CUI: C3887873
Disease: Hearing Loss
0.700 GeneticVariation CLINVAR
Hearing Loss
CUI: C3887873
Disease: Hearing Loss
0.700 CausalMutation CLINVAR