List of variants in gene COQ8B reported as benign by Mayo Clinic Laboratories, Mayo Clinic

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_024876.4(COQ8B):c.1035+7T>C	rs2246095	0.56103
NM_024876.4(COQ8B):c.521A>G (p.His174Arg)	rs3865452	0.47243
NM_024876.4(COQ8B):c.768G>A (p.Ala256=)	rs11538385	0.22464
NM_024876.4(COQ8B):c.9G>A (p.Leu3=)	rs11673492	0.16347
NM_024876.4(COQ8B):c.648C>T (p.Ala216=)	rs4803357	0.02373
NM_024876.4(COQ8B):c.1119C>T (p.Phe373=)	rs56056214	0.01001

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