RS1465930949 VMA21

Health Risk Chr X:151397319
Upload your DNA to see your genotype for this variant.
Associated Conditions
X-linked myopathy with excessive autophagy
Inborn genetic diseases
X-linked myopathy with excessive autophagy
Inborn genetic diseases
Other Variants in VMA21
rs797044909 rs878854352 rs878854353 rs878854354 rs878854355 rs878854356 rs1556035617 rs878854357 rs765120199 rs143565725
Ask Dr. Hemsworth about this variant