RS201587138 LOXHD1

Health Risk Chr 18:46529227
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What This Variant Does
"CLNSIG=255
Associated Conditions
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 77
Nonsyndromic genetic hearing loss
LOXHD1-related disorder
Inborn genetic diseases
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 77
Nonsyndromic genetic hearing loss
LOXHD1-related disorder
Inborn genetic diseases
Other Variants in LOXHD1
rs121918370 rs75949023 rs187658135 rs140437150 rs35007621 rs199804946 rs34589386 rs35088381 rs35727744 rs367826075
Ask Dr. Hemsworth about this variant