RS370898981 TMC1

Health Risk Chr 9:72816213
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 7
Autosomal dominant nonsyndromic hearing loss 36
Nonsyndromic genetic hearing loss
Monogenic hearing loss
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 7
Autosomal dominant nonsyndromic hearing loss 36
Nonsyndromic genetic hearing loss
Monogenic hearing loss
Other Variants in TMC1
rs121908072 rs121908073 rs121908074 rs1169090943 rs121908076 rs397517834 rs151001642 rs140388347 rs11143384 rs370088722
Ask Dr. Hemsworth about this variant