RS587777585 VARS2

Health Risk Chr 6:30918851
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What This Variant Does
"CLNSIG=5
Associated Conditions
Combined oxidative phosphorylation defect type 20
Inborn genetic diseases
Combined oxidative phosphorylation defect type 20
Inborn genetic diseases
Other Variants in VARS2
rs587777583 rs587777584 rs138855624 rs139515727 rs775439829 rs1554268077 rs200168128 rs367960344 rs202201763 rs778868393
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