List of variants in gene NDUFAF2 reported as likely pathogenic by GeneDx

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_174889.5(NDUFAF2):c.131A>C (p.Gln44Pro)	rs775605330	0.00007
NM_174889.5(NDUFAF2):c.221G>A (p.Trp74Ter)	rs772294726	0.00001
NM_174889.5(NDUFAF2):c.79C>T (p.Gln27Ter)	rs1554076318

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