ClinVar Miner

List of variants in gene NDUFAF2 reported as likely 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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_174889.5(NDUFAF2):c.462T>C (p.Phe154=)	rs77878573	0.01828
NM_174889.5(NDUFAF2):c.300A>T (p.Ile100=)	rs191388646	0.00585

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