RS104894403 GJB2
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What This Variant Does
"[OMIM:?]
Associated Conditions
Hearing loss
Mutilating keratoderma
Sensorineural hearing loss disorder
Autosomal dominant nonsyndromic hearing loss 3A
Autosomal recessive nonsyndromic hearing loss 1A
Ichthyosis
hystrix-like
with hearing loss
Hearing loss
Mutilating keratoderma
Sensorineural hearing loss disorder
Autosomal dominant nonsyndromic hearing loss 3A
Autosomal recessive nonsyndromic hearing loss 1A
Ichthyosis
hystrix-like
Other Variants in GJB2