List of variants in gene NCF2 reported as uncertain significance for Chronic granulomatous disease

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: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000433.4(NCF2):c.*517dup	rs573207861	0.00065
NM_000433.4(NCF2):c.*445A>C	rs886045647	0.00001
NM_000433.4(NCF2):c.*264AG[2]	rs886045650
NM_000433.4(NCF2):c.*393del	rs771465757
NM_000433.4(NCF2):c.*393dup	rs771465757
NM_000433.4(NCF2):c.397_398insTCA	rs886045648
NM_000433.4(NCF2):c.508_512dup	rs555649211
NM_000433.4(NCF2):c.*510T>A	rs886045646
NM_000433.4(NCF2):c.*539GTTT[1]	rs376681445

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.