RS117385606 GJB3

Health Risk Chr 1:34785342
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What This Variant Does
"[OMIM:?]
Associated Conditions
Deafness
digenic
GJB2/GJB3
Erythrokeratodermia variabilis et progressiva 1
Autosomal recessive nonsyndromic hearing loss 1A
Autosomal dominant nonsyndromic hearing loss 2B
Deafness
digenic
GJB2/GJB3
Erythrokeratodermia variabilis et progressiva 1
Autosomal recessive nonsyndromic hearing loss 1A
Autosomal dominant nonsyndromic hearing loss 2B
Other Variants in GJB3
rs74315315 rs74315316 rs74315317 rs74315318 rs74315321 rs786200895 rs28937583 rs199689484 rs376506263 rs201314683
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