RS727503326 MYO6
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 22
Autosomal recessive nonsyndromic hearing loss 37
Inborn genetic diseases
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 22
Autosomal recessive nonsyndromic hearing loss 37
Inborn genetic diseases
Other Variants in MYO6