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i6011292

From SNPedia

23andMe dataI6011292
23andMe searchI6011292
opensnpI6011292
Gene (via rs)GJB2

aliasrs111033295
Rs_StabilizedOrientationminus
RsGeno Mag Summary
(A;A) 0 common in clinvar
(A;T) 3 Carrier of a recessive deafness mutation

rs111033295

recessive GJB2 gene variant associated with deafness