ClinVar Miner

List of variants in gene combination COQ2, LOC112997540 reported as benign for coenzyme Q10 deficiency

Included ClinVar conditions (13):

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)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001358921.2(COQ2):c.46G>T (p.Val16Leu)	rs6818847	0.62431
NM_015697.9(COQ2):c.30G>A (p.Arg10=)	rs183012002	0.00375

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