RS111033349 OTOF

Health Risk Chr 2:26461854
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What This Variant Does
"CLNSIG=4
Associated Conditions
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 9
Nonsyndromic genetic hearing loss
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 9
Nonsyndromic genetic hearing loss
Other Variants in OTOF
rs80356600 rs80356584 rs2148047884 rs80356605 rs80356593 rs28937591 rs80356602 rs121908598 rs80356596 rs80356586
Ask Dr. Hemsworth about this variant