List of variants reported as benign for Neutrophil immunodeficiency syndrome by Labcorp Genetics (formerly Invitae), Labcorp

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_002872.5(RAC2):c.477T>C (p.Ala159=)	rs1064498	0.22300
NM_002872.5(RAC2):c.81C>G (p.Ala27=)	rs2239774	0.15604
NM_002872.5(RAC2):c.107+20T>C	rs6000622	0.06966
NM_002872.5(RAC2):c.252C>T (p.Leu84=)	rs2230919	0.02042
NM_002872.5(RAC2):c.449-18G>T	rs73889256	0.00403
NM_002872.5(RAC2):c.35+16G>A	rs200969255	0.00209
NM_002872.5(RAC2):c.501C>T (p.Thr167=)	rs79799102	0.00067
NM_002872.5(RAC2):c.226-21dup	rs11374583
NM_002872.5(RAC2):c.448+11C>T	rs530853255

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.