RS184435771 MYO15A

Health Risk Chr 17:18154714
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Inborn genetic diseases
Autosomal recessive nonsyndromic hearing loss 3
Hearing impairment
Monogenic hearing loss
Rare genetic deafness
Inborn genetic diseases
Autosomal recessive nonsyndromic hearing loss 3
Hearing impairment
Monogenic hearing loss
Other Variants in MYO15A
rs121908965 rs121908966 rs121908967 rs121908968 rs748108031 rs121908969 rs121908971 rs769884586 rs121908972 rs746051220
Ask Dr. Hemsworth about this variant