List of variants in gene NDUFB3 reported as pathogenic for Mitochondrial complex 1 deficiency, nuclear type 25

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_002491.3(NDUFB3):c.64T>C (p.Trp22Arg)	rs142609245	0.00116
NM_002491.3(NDUFB3):c.208G>T (p.Gly70Ter)	rs200800978	0.00016
NM_002491.3(NDUFB3):c.117del (p.Gly40_Leu41insTer)	rs2125534778

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