List of variants in gene COQ9 reported as likely benign for Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_020312.4(COQ9):c.921+13C>T	rs115677652	0.01317
NM_020312.4(COQ9):c.379-16G>C	rs62037144	0.00308
NM_020312.4(COQ9):c.826C>T (p.Arg276Trp)	rs143587648	0.00290
NM_020312.4(COQ9):c.625C>G (p.Leu209Val)	rs78846023	0.00217
NM_020312.4(COQ9):c.*100C>T	rs373048666	0.00149
NM_020312.4(COQ9):c.921+11C>A	rs75908124	0.00146
NM_020312.4(COQ9):c.240C>G (p.Pro80=)	rs2301773	0.00003
NM_020312.4(COQ9):c.337G>A (p.Ala113Thr)	rs377307935	0.00001
NM_020312.4(COQ9):c.79C>G (p.Arg27Gly)	rs140264612

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