RS876657653 MYO6

Health Risk Chr 6:75890237
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What This Variant Does
"CLNSIG=4
Associated Conditions
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 37
Autosomal dominant nonsyndromic hearing loss 22
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 37
Autosomal dominant nonsyndromic hearing loss 22
Other Variants in MYO6
rs121912557 rs1562201376 rs121912558 rs121912559 rs121912560 rs121912561 rs1562283089 rs199798449 rs144031818 rs111033431
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