List of variants in gene combination CARS2, LOC130010127 reported as benign 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_024537.3(CARS2):c.-48C>T	rs3818496	0.59027
NM_024537.4(CARS2):c.64G>A (p.Gly22Arg)	rs534818713	0.00328

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