RS121908072 TMC1

Health Risk Chr 9:72816161
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 36
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 36
Monogenic hearing loss
Autosomal dominant nonsyndromic hearing loss 36
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 36
Monogenic hearing loss
Other Variants in TMC1
rs121908073 rs121908074 rs1169090943 rs121908076 rs397517834 rs151001642 rs140388347 rs370898981 rs11143384 rs370088722
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