RS121908073 TMC1

Health Risk Chr 9:72694578
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 7
Rare genetic deafness
Hearing loss
autosomal recessive
Autosomal dominant nonsyndromic hearing loss 36
Autosomal recessive nonsyndromic hearing loss 7
Rare genetic deafness
Hearing loss
autosomal recessive
Autosomal dominant nonsyndromic hearing loss 36
Other Variants in TMC1
rs121908072 rs121908074 rs1169090943 rs121908076 rs397517834 rs151001642 rs140388347 rs370898981 rs11143384 rs370088722
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