RS765120199 VMA21

Health Risk Chr X:151397323
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Associated Conditions
X-linked myopathy with excessive autophagy
Inborn genetic diseases
VMA21-related disorder
X-linked myopathy with excessive autophagy
Inborn genetic diseases
VMA21-related disorder
Other Variants in VMA21
rs797044909 rs878854352 rs878854353 rs878854354 rs878854355 rs878854356 rs1556035617 rs878854357 rs143565725 rs1465930949
Ask Dr. Hemsworth about this variant