RS104894397 GJB2
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 1A
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 3A
Autosomal recessive nonsyndromic hearing loss 1B
Nonsyndromic genetic hearing loss
Hearing impairment
GJB2-related disorder
7 conditions
Autosomal recessive nonsyndromic hearing loss 1A
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 3A
Autosomal recessive nonsyndromic hearing loss 1B
Nonsyndromic genetic hearing loss
Hearing impairment
GJB2-related disorder
Other Variants in GJB2