RS1345580310 MYO15A

Health Risk Chr 17:18167686
Upload your DNA to see your genotype for this variant.
Associated Conditions
Rare genetic deafness
Inborn genetic diseases
Nonsyndromic genetic hearing loss
Rare genetic deafness
Inborn genetic diseases
Nonsyndromic genetic hearing loss
Other Variants in MYO15A
rs121908965 rs121908966 rs121908967 rs121908968 rs748108031 rs121908969 rs121908971 rs769884586 rs121908972 rs746051220
Ask Dr. Hemsworth about this variant