RS104894409 GJB2
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 1A
Hearing impairment
Rare genetic deafness
Nonsyndromic genetic hearing loss
8 conditions
GJB2-related disorder
Autosomal recessive nonsyndromic hearing loss 1A
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 3A
Progressive sensorineural hearing impairment
GJB2-related disorder
Autosomal recessive nonsyndromic hearing loss 1A
Autosomal recessive nonsyndromic hearing loss 1A
Hearing impairment
Rare genetic deafness
Other Variants in GJB2