List of variants in gene combination ATPAF2, LOC130060411 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_145691.4(ATPAF2):c.-90C>A	rs113286105	0.00040
NM_145691.4(ATPAF2):c.-85C>T	rs533220549	0.00033
NM_145691.4(ATPAF2):c.-107G>T	rs371822840

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