rs117685390, GJB2

N. diseases: 1
Disease: Nonsyndromic Deafness ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Nonsyndromic Deafness
CUI: C3711374
Disease: Nonsyndromic Deafness
0.010 GeneticVariation BEFREE These results suggest that the rs117685390 C allele could represent a biomarker for the development of NSHI in Caucasian populations and may be included in risk assessment for the development of NSHI. 23640091 2013