List of variants in gene NCF4 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000631.5(NCF4):c.478G>A (p.Val160Met)	rs150103256	0.00121
NM_000631.5(NCF4):c.172C>T (p.Arg58Cys)	rs143532979	0.00103
NM_000631.5(NCF4):c.271+6C>T	rs200052796	0.00036
NM_000631.5(NCF4):c.906C>T (p.Asp302=)	rs567611718	0.00013
NM_000631.5(NCF4):c.306C>T (p.Ala102=)	rs34072404	0.00005
NM_000631.5(NCF4):c.471-9T>C	rs765278988	0.00005

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