Gene: GJB3 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs144964568
rs144964568
GJB3 ; SMIM12 ; LOC105378642
T 0.700 GeneticVariation CLINVAR

dbSNP: rs749431664
rs749431664
GJB3 ; SMIM12 ; LOC105378642
0.010 GeneticVariation BEFREE Mechanism of a novel missense mutation, p.V174M, of the human connexin31 (GJB3) in causing nonsyndromic hearing loss. 24913888

2014