List of variants in gene NCF4 reported as not provided

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.758+57T>C	rs2075939	0.86715
NM_000631.5(NCF4):c.647C>T (p.Thr216Met)	rs146911421	0.00064
NM_000631.5(NCF4):c.314G>A (p.Arg105Gln)	rs387906808	0.00003
NM_000631.5(NCF4):c.143_152dup (p.Lys52fs)	rs869025585	0.00002

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