RS746724027 TMC1

Health Risk Chr 9:72788422
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Associated Conditions
Autosomal dominant nonsyndromic hearing loss 36
Inborn genetic diseases
TMC1-related disorder
Monogenic hearing loss
Autosomal dominant nonsyndromic hearing loss 36
Inborn genetic diseases
TMC1-related disorder
Monogenic hearing loss
Other Variants in TMC1
rs121908072 rs121908073 rs121908074 rs1169090943 rs121908076 rs397517834 rs151001642 rs140388347 rs370898981 rs11143384
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