RS876657727 TMC1

Health Risk Chr 9:72791896
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 36
Autosomal recessive nonsyndromic hearing loss 7
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 36
Autosomal recessive nonsyndromic hearing loss 7
Other Variants in TMC1
rs121908072 rs121908073 rs121908074 rs1169090943 rs121908076 rs397517834 rs151001642 rs140388347 rs370898981 rs11143384
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