RS878853225 MYO6

Health Risk Chr 6:75858993
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 22
Autosomal dominant nonsyndromic hearing loss 22
Other Variants in MYO6
rs121912557 rs1562201376 rs121912558 rs121912559 rs121912560 rs121912561 rs1562283089 rs199798449 rs144031818 rs111033431
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