RS140236996 TECTA

Health Risk Chr 11:121168064
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 12
Inborn genetic diseases
Rare genetic deafness
See cases
Monogenic hearing loss
Autosomal dominant nonsyndromic hearing loss 12
Inborn genetic diseases
Rare genetic deafness
See cases
Monogenic hearing loss
Other Variants in TECTA
rs121909058 rs966621865 rs121909059 rs121909060 rs1591437831 rs1281790755 rs121909061 rs121909062 rs121909063 rs1591462832
Ask Dr. Hemsworth about this variant