RS111033253 GJB2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 1A
Hearing impairment
Rare genetic deafness
Hearing loss
Autosomal recessive nonsyndromic hearing loss 1B
Nonsyndromic genetic hearing loss
7 conditions
Mutilating keratoderma
Palmoplantar keratoderma-deafness syndrome
Knuckle pads
deafness AND leukonychia syndrome
Monogenic hearing loss
Autosomal recessive nonsyndromic hearing loss 1A
Hearing impairment
Rare genetic deafness
Other Variants in GJB2