RS75949023 LOXHD1

Health Risk Chr 18:46524734
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 77
Rare genetic deafness
LOXHD1-related disorder
Deafness
Autosomal recessive nonsyndromic hearing loss 77
Rare genetic deafness
LOXHD1-related disorder
Deafness
Other Variants in LOXHD1
rs121918370 rs187658135 rs140437150 rs35007621 rs199804946 rs34589386 rs35088381 rs35727744 rs367826075 rs199595156
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