RS766753922 OTOGL

Health Risk Chr 12:80239362
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 84B
Meniere disease
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 84B
Meniere disease
Other Variants in OTOGL
rs1233562246 rs397514588 rs902734999 rs876657658 rs200050988 rs78377084 rs192234924 rs76420383 rs192944055 rs199855270
Ask Dr. Hemsworth about this variant