Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80338941
rs80338941
GJB2
0.710 GeneticVariation BEFREE The screening of the candidate genes for deafness and/or cataract allowed us to identify two variants, M34T and S19T, of the GJB2 gene in family members with hearing impairment. 16077952

2005
dbSNP: rs80338941
rs80338941
GJB2
G 0.710 CausalMutation CLINVAR