RS80338950 GJB2
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 1A
Rare genetic deafness
Hearing loss
8 conditions
Autosomal dominant nonsyndromic hearing loss 3A
Nonsyndromic genetic hearing loss
7 conditions
Autosomal dominant nonsyndromic hearing loss 3A
Hearing impairment
Hearing loss
Rare genetic deafness
Nonsyndromic genetic hearing loss
Autosomal recessive nonsyndromic hearing loss 1A
Autosomal recessive nonsyndromic hearing loss 1A
Rare genetic deafness
Other Variants in GJB2