RS104894407 GJB2
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 3A
Hearing impairment
Autosomal recessive nonsyndromic hearing loss 1A
Autosomal dominant nonsyndromic hearing loss 3A
Hearing impairment
Autosomal recessive nonsyndromic hearing loss 1A
Other Variants in GJB2