RS727504567 MYO6

Health Risk Chr 6:75828590
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What This Variant Does
"CLNSIG=4
Associated Conditions
Nonsyndromic genetic hearing loss
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 22
Monogenic hearing loss
Nonsyndromic genetic hearing loss
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 22
Monogenic hearing loss
Other Variants in MYO6
rs121912557 rs1562201376 rs121912558 rs121912559 rs121912560 rs121912561 rs1562283089 rs199798449 rs144031818 rs111033431
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