List of variants in gene combination LOC112552175, NDUFA11 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_175614.4(NDUFA11):c.-217A>G	rs1056987	0.68730
NM_175614.4(NDUFA11):c.-88C>A	rs8108064	0.64945

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