RS80338948 GJB2
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 1A
Hearing impairment
Rare genetic deafness
Hearing loss
7 conditions
Autosomal dominant nonsyndromic hearing loss 3A
Nonsyndromic genetic hearing loss
GJB2-related disorder
Palmoplantar keratoderma-deafness syndrome
Knuckle pads
deafness AND leukonychia syndrome
Mutilating keratoderma
Autosomal recessive nonsyndromic hearing loss 1A
Hearing impairment
Rare genetic deafness
Other Variants in GJB2