RS786200895 GJB3

Health Risk Chr 1:34784956
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What This Variant Does
"CLNSIG=5
Associated Conditions
Deafness
autosomal dominant
with peripheral neuropathy
Hearing impairment
Deafness
autosomal dominant
with peripheral neuropathy
Hearing impairment
Other Variants in GJB3
rs74315315 rs74315316 rs74315317 rs74315318 rs74315321 rs28937583 rs117385606 rs199689484 rs376506263 rs201314683
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