RS587783791 MTM1

Health Risk Chr X:150598594
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Severe X-linked myotubular myopathy
MTM1-related disorder
Centronuclear myopathy
Severe X-linked myotubular myopathy
MTM1-related disorder
Centronuclear myopathy
Other Variants in MTM1
rs132630302 rs132630303 rs132630304 rs672601324 rs397518445 rs132630305 rs132630306 rs672601325 rs132630307 rs398123264
Ask Dr. Hemsworth about this variant