List of variants in gene combination ERCC8, NDUFAF2 reported as benign for congenital myopathy

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_174889.4(NDUFAF2):c.-97A>G	rs158922	0.66969
NM_174889.5(NDUFAF2):c.60G>A (p.Lys20=)	rs158921	0.63042

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