RS121918232 COQ2

Health Risk Chr 4:83273505
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What This Variant Does
"[OMIM:?]
Associated Conditions
Coenzyme Q10 deficiency
primary
1
Nephrotic syndrome
Inborn genetic diseases
Coenzyme Q10 deficiency
primary
1
Nephrotic syndrome
Inborn genetic diseases
Other Variants in COQ2
rs121918230 rs121918231 rs121918233 rs778094136 rs397514727 rs751185256 rs745619253 rs761785906 rs863223936 rs368891722
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