RS779018464 GJB2
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What This Variant Does
"CLNSIG=4
Associated Conditions
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 3A
Autosomal recessive nonsyndromic hearing loss 1A
Nonsyndromic genetic hearing loss
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 3A
Autosomal recessive nonsyndromic hearing loss 1A
Nonsyndromic genetic hearing loss
Other Variants in GJB2