RS76434661 GJB2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Hearing impairment
Autosomal recessive nonsyndromic hearing loss 1A
Autosomal dominant nonsyndromic hearing loss 3A
8 conditions
Hearing loss
Autosomal recessive nonsyndromic hearing loss 1B
7 conditions
Intellectual disability
Mutilating keratoderma
Palmoplantar keratoderma-deafness syndrome
Knuckle pads
deafness AND leukonychia syndrome
Rare genetic deafness
Hearing impairment
Other Variants in GJB2