RS587783772 MTM1

Health Risk Chr X:150659665
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What This Variant Does
"CLNSIG=5
Associated Conditions
Severe X-linked myotubular myopathy
Spastic paraplegia
Centronuclear myopathy
Congenital myopathy with fiber type disproportion
Inborn genetic diseases
Severe X-linked myotubular myopathy
Spastic paraplegia
Centronuclear myopathy
Congenital myopathy with fiber type disproportion
Inborn genetic diseases
Other Variants in MTM1
rs132630302 rs132630303 rs132630304 rs672601324 rs587783791 rs397518445 rs132630305 rs132630306 rs672601325 rs132630307
Ask Dr. Hemsworth about this variant