Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs780320724
rs780320724
GJB6
0.010 GeneticVariation BEFREE These findings suggest that the p.A40V mutation in CX30 causes autosomal-dominant nonsyndromic hearing loss. 21731760

2011