RS760980785 MYO15A

Health Risk Chr 17:18146035
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What This Variant Does
"CLNSIG=4
Associated Conditions
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 3
Monogenic hearing loss
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 3
Monogenic hearing loss
Other Variants in MYO15A
rs121908965 rs121908966 rs121908967 rs121908968 rs748108031 rs121908969 rs121908971 rs769884586 rs121908972 rs746051220
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