List of variants in gene NDUFS2 reported as benign for Mitochondrial complex I deficiency, nuclear type 1

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001377299.1(NDUFS2):c.*114A>G	rs1136224	0.13305
NM_001377299.1(NDUFS2):c.1290C>T (p.Ala430=)	rs1136207	0.11971
NM_004550.5(NDUFS2):c.-388G>T	rs3813623	0.11879

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