RS104894398 GJB2
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 1A
Hearing impairment
Rare genetic deafness
Hearing loss
Nonsyndromic genetic hearing loss
GJB2-related disorder
7 conditions
Autosomal recessive nonsyndromic hearing loss 1A
Hearing impairment
Rare genetic deafness
Hearing loss
Nonsyndromic genetic hearing loss
GJB2-related disorder
7 conditions
Other Variants in GJB2