RS786204734 GJB2
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What This Variant Does
"CLNSIG=4
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 1A
Rare genetic deafness
Hearing loss
Nonsyndromic genetic hearing loss
7 conditions
Palmoplantar keratoderma-deafness syndrome
Mutilating keratoderma
Knuckle pads
deafness AND leukonychia syndrome
Autosomal recessive nonsyndromic hearing loss 1A
Rare genetic deafness
Hearing loss
Nonsyndromic genetic hearing loss
7 conditions
Palmoplantar keratoderma-deafness syndrome
Other Variants in GJB2