ClinVar Miner

List of variants in gene COQ2 reported as benign for Coenzyme Q10 deficiency, primary, 1

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001358921.2(COQ2):c.744T>C (p.Asp248=)	rs6535454	0.74903
NM_001358921.2(COQ2):c.840C>T (p.Ser280=)	rs1129617	0.22636

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