ClinVar Miner

List of variants in gene COQ2 reported as uncertain significance for Coenzyme Q10 deficiency

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001358921.2(COQ2):c.*257T>C	rs746613612	0.00003
NM_001358921.2(COQ2):c.*348dup	rs542593202

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