List of variants in gene combination NDUFA2, TMCO6 reported as benign for hereditary skeletal muscle disorder

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_002488.4(NDUFA2):c.-136A>G	rs778594	0.38702
NM_002488.4(NDUFA2):c.-48A>G	rs778593	0.38666

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