RS767298430 COQ2

Health Risk Chr 4:83284866
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What This Variant Does
"CLNSIG=5
Associated Conditions
Focal segmental glomerulosclerosis
Inborn genetic diseases
Coenzyme Q10 deficiency
primary
1
Multiple system atrophy 1
susceptibility to
Focal segmental glomerulosclerosis
Inborn genetic diseases
Coenzyme Q10 deficiency
primary
1
Multiple system atrophy 1
susceptibility to
Other Variants in COQ2
rs121918230 rs121918231 rs121918232 rs121918233 rs778094136 rs397514727 rs751185256 rs745619253 rs761785906 rs863223936
Ask Dr. Hemsworth about this variant