List of variants in gene COQ4 reported as likely pathogenic for Inborn genetic diseases

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_016035.5(COQ4):c.202G>C (p.Asp68His)	rs758522459	0.00007
NM_016035.5(COQ4):c.469C>A (p.Gln157Lys)	rs1045118320	0.00001
NM_016035.5(COQ4):c.55C>T (p.Gln19Ter)	rs1832230836	0.00001

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