RS111033373 OTOF

Health Risk Chr 2:26462181 snv splice acceptor variant
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
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
Population Frequencies
gnomAD ALL
0%
Other Variants in OTOF
rs80356600 rs80356584 rs2148047884 rs80356605 rs80356593 rs28937591 rs80356602 rs121908598 rs80356596 rs80356586
Ask Dr. Hemsworth about this variant