RS878854357 VMA21

Health Risk Chr X:151403611
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
X-linked myopathy with excessive autophagy
X-linked myopathy with excessive autophagy
Other Variants in VMA21
rs797044909 rs878854352 rs878854353 rs878854354 rs878854355 rs878854356 rs1556035617 rs765120199 rs143565725 rs1465930949
Ask Dr. Hemsworth about this variant