List of variants in gene SLC25A26 reported as 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001379210.1(SLC25A26):c.623C>T (p.Thr208Met)	rs13874	0.57380
NM_001379210.1(SLC25A26):c.498+13G>A	rs332354	0.54714
NM_001379210.1(SLC25A26):c.122G>A (p.Ser41Asn)	rs146159281	0.43643
NM_001379210.1(SLC25A26):c.*3C>A	rs116677829	0.02088

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