RS373937326 LOXHD1

Health Risk Chr 18:46534448
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 77
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 77
Other Variants in LOXHD1
rs121918370 rs75949023 rs187658135 rs140437150 rs35007621 rs199804946 rs34589386 rs35088381 rs35727744 rs367826075
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