RS28938175 COCH
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What This Variant Does
"deafness [OMIM:DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 9]
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 9
Nonsyndromic genetic hearing loss
Rare genetic deafness
Hearing impairment
Autosomal dominant nonsyndromic hearing loss 9
Nonsyndromic genetic hearing loss
Rare genetic deafness
Hearing impairment
Other Variants in COCH