RS111033293 GJB2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 1A
Rare genetic deafness
8 conditions
Nonsyndromic genetic hearing loss
Monogenic hearing loss
Autosomal recessive nonsyndromic hearing loss 1A
Nonsyndromic genetic hearing loss
Autosomal recessive nonsyndromic hearing loss 1A
Rare genetic deafness
8 conditions
Nonsyndromic genetic hearing loss
Monogenic hearing loss
Autosomal recessive nonsyndromic hearing loss 1A
Nonsyndromic genetic hearing loss
Other Variants in GJB2