List of variants in gene combination MPHOSPH9, MTRFR 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_152269.5(MTRFR):c.-51C>T	rs115161149	0.00062
NM_152269.4(MTRFR):c.-128C>T	rs886049039	0.00002
NM_152269.4(MTRFR):c.-132A>G	rs1025491766	0.00001
NM_152269.4(MTRFR):c.-206G>T	rs886049038	0.00001
NM_152269.4(MTRFR):c.-166T>C	rs1314198112

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