List of variants in gene combination LOC130065433, NDUFAF5 reported as likely benign for Mitochondrial complex I deficiency

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_024120.5(NDUFAF5):c.183G>C (p.Arg61=)	rs139219896	0.00468
NM_024120.5(NDUFAF5):c.9G>A (p.Arg3=)	rs201860210	0.00011
NM_024120.5(NDUFAF5):c.130C>T (p.Leu44=)	rs768309175	0.00004

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