RS397516335 POU3F4
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What This Variant Does
"CLNSIG=4
Associated Conditions
Rare genetic deafness
X-linked mixed hearing loss with perilymphatic gusher
Nonsyndromic genetic hearing loss
Rare genetic deafness
X-linked mixed hearing loss with perilymphatic gusher
Nonsyndromic genetic hearing loss
Other Variants in POU3F4