ClinVar Miner

List of variants in gene combination COQ9, LOC112469007 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_020312.3(COQ9):c.-37C>G	rs886052178	0.00010
NM_020312.4(COQ9):c.-25C>T	rs547268811
NM_020312.4(COQ9):c.73+9del	rs749532852

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