RS372710475 TMC1

Health Risk Chr 9:72791994
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Rare genetic deafness
Hearing loss
autosomal recessive
Autosomal dominant nonsyndromic hearing loss 36
TMC1-related disorder
Nonsyndromic genetic hearing loss
Rare genetic deafness
Hearing loss
autosomal recessive
Autosomal dominant nonsyndromic hearing loss 36
TMC1-related disorder
Nonsyndromic genetic hearing loss
Other Variants in TMC1
rs121908072 rs121908073 rs121908074 rs1169090943 rs121908076 rs397517834 rs151001642 rs140388347 rs370898981 rs11143384
Ask Dr. Hemsworth about this variant