RS121908969 MYO15A

Health Risk Chr 17:18154190
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 3
Autosomal recessive nonsyndromic hearing loss 3
Other Variants in MYO15A
rs121908965 rs121908966 rs121908967 rs121908968 rs748108031 rs121908971 rs769884586 rs121908972 rs746051220 rs1270302810
Ask Dr. Hemsworth about this variant