RS370730786 OTOGL

Health Risk Chr 12:80302784
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What This Variant Does
"CLNSIG=4
Associated Conditions
OTOGL-related disorder
Inborn genetic diseases
Autosomal recessive nonsyndromic hearing loss 84B
OTOGL-related disorder
Inborn genetic diseases
Autosomal recessive nonsyndromic hearing loss 84B
Other Variants in OTOGL
rs1233562246 rs397514588 rs902734999 rs876657658 rs200050988 rs766753922 rs78377084 rs192234924 rs76420383 rs192944055
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