ClinVar Miner

List of variants reported as likely pathogenic for coenzyme Q10 deficiency by SingHealth Duke-NUS Institute of Precision Medicine

Included ClinVar conditions (13):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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.440G>A (p.Arg147His)	rs121918231	0.00003
NM_020247.5(COQ8A):c.*72dup	rs1558212305

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