List of variants in gene combination AIFM1, LOC126863317, RAB33A reported as likely benign for combined oxidative phosphorylation deficiency

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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_004208.4(AIFM1):c.605+14T>C	rs368859964	0.00011
NM_004208.4(AIFM1):c.605+9G>T	rs1191297439	0.00001
NM_004208.4(AIFM1):c.605+13A>G

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