List of variants in gene NDUFS4 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_002495.4(NDUFS4):c.198A>C (p.Gly66=)	rs31304	0.96579
NM_002495.4(NDUFS4):c.312A>G (p.Arg104=)	rs31303	0.79100
NM_002495.4(NDUFS4):c.*46G>A	rs567	0.42121
NM_002495.4(NDUFS4):c.424+19dup	rs140172554

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