RS377389290 MYO15A

Health Risk Chr 17:18157749
Upload your DNA to see your genotype for this variant.
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 3
Inborn genetic diseases
Autosomal recessive nonsyndromic hearing loss 3
Inborn genetic diseases
Other Variants in MYO15A
rs121908965 rs121908966 rs121908967 rs121908968 rs748108031 rs121908969 rs121908971 rs769884586 rs121908972 rs746051220
Ask Dr. Hemsworth about this variant