Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs72474224
rs72474224
GJB2
CUI: C1384666
Disease: hearing impairment
hearing impairment 		T 0.800 GeneticVariation CLINVAR

dbSNP: rs72474224
rs72474224
GJB2
CUI: C1384666
Disease: hearing impairment
hearing impairment 		T 0.800 CausalMutation CLINVAR