List of variants in gene COQ9 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_020312.4(COQ9):c.826C>T (p.Arg276Trp)	rs143587648	0.00290
NM_020312.4(COQ9):c.835G>A (p.Asp279Asn)	rs76508383	0.00282
NM_020312.4(COQ9):c.625C>G (p.Leu209Val)	rs78846023	0.00217
NM_020312.4(COQ9):c.867+7G>A	rs1251079428

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