RS121912558 MYO6

Health Risk Chr 6:75914119
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 37
Autosomal recessive nonsyndromic hearing loss 37
Other Variants in MYO6
rs121912557 rs1562201376 rs121912559 rs121912560 rs121912561 rs1562283089 rs199798449 rs144031818 rs111033431 rs397517045
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