List of variants in gene NCF4 reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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_000631.5(NCF4):c.758+57T>C	rs2075939	0.86715
NM_000631.5(NCF4):c.897G>A (p.Ser299=)	rs11552115	0.12037
NM_000631.5(NCF4):c.735C>T (p.Tyr245=)	rs2072712	0.11870

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