List of variants in gene NDUFS1 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_005006.7(NDUFS1):c.*336G>T	rs1044120	0.52989
NM_005006.7(NDUFS1):c.1251A>G (p.Arg417=)	rs1801318	0.34874
NM_005006.7(NDUFS1):c.*733A>G	rs6707707	0.03241
NM_005006.7(NDUFS1):c.*457T>A	rs4147728
NM_005006.7(NDUFS1):c.966G>T (p.Ala322=)	rs1127566

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