Variants in gene COQ8A with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 6

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HGVS	dbSNP	gnomAD frequency
NM_020247.5(COQ8A):c.63G>A (p.Ala21=)	rs11549709	0.01280
NM_020247.5(COQ8A):c.989A>G (p.Tyr330Cys)	rs150243147	0.00127
NM_020247.5(COQ8A):c.67G>A (p.Val23Met)	rs35582308	0.00058
NM_020247.5(COQ8A):c.258A>C (p.Ala86=)	rs137872711	0.00043
NM_020247.5(COQ8A):c.1258G>A (p.Asp420Asn)	rs147097934	0.00014
NM_020247.5(COQ8A):c.697G>A (p.Ala233Thr)	rs376462712

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