RS104894401 GJB2
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 1A
Autosomal dominant nonsyndromic hearing loss 3A
7 conditions
Nonsyndromic genetic hearing loss
Autosomal recessive nonsyndromic hearing loss 1A
Autosomal dominant nonsyndromic hearing loss 3A
7 conditions
Nonsyndromic genetic hearing loss
Other Variants in GJB2