List of variants in gene combination AVIL, TSFM reported as uncertain significance for combined oxidative phosphorylation 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)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_005726.6(TSFM):c.*895A>G	rs58949411	0.00002
NM_005726.6(TSFM):c.*866T>G	rs1397583217	0.00001

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