List of variants in gene NCF4 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000631.5(NCF4):c.172C>T (p.Arg58Cys)	rs143532979	0.00103
NM_000631.5(NCF4):c.759-7C>A	rs146292447	0.00025
NM_000631.5(NCF4):c.758+32G>A	rs148129899	0.00016
NM_000631.5(NCF4):c.451C>T (p.Arg151Cys)	rs150976323	0.00007

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