List of variants in gene combination NCAPH2, SCO2 reported as likely benign for Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1

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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_005138.3(SCO2):c.763C>A (p.Arg255=)	rs112793292	0.00755
NM_005138.3(SCO2):c.201C>T (p.Phe67=)	rs61748568	0.00240
NM_005138.3(SCO2):c.576C>T (p.Thr192=)	rs201909075	0.00035

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