List of variants in gene NDUFV1 reported as benign for mitochondrial complex deficiency

Minimum submission review status:		Collection method:
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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_007103.4(NDUFV1):c.1056T>C (p.Ala352=)	rs11227859	0.05117
NM_007103.4(NDUFV1):c.549C>G (p.Gly183=)	rs10896187	0.05020

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