RS111033190 GJB2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 1A
Autosomal dominant nonsyndromic hearing loss 3A
nonsyndromic sensorineural hearing loss
GJB2-related disorder
Monogenic hearing loss
Autosomal recessive nonsyndromic hearing loss 1A
Hearing loss
Nonsyndromic genetic hearing loss
8 conditions
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 1A
Autosomal dominant nonsyndromic hearing loss 3A
nonsyndromic sensorineural hearing loss
GJB2-related disorder
Other Variants in GJB2