List of variants in gene ITGB2 reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000211.5(ITGB2):c.1323T>C (p.Val441=)	rs235326	0.74399
NM_000211.5(ITGB2):c.1101C>A (p.Val367=)	rs2230529	0.23426
NM_000211.5(ITGB2):c.819G>A (p.Gly273=)	rs2230528	0.21986
NM_000211.5(ITGB2):c.328+15G>A	rs5030668	0.13213
NM_000211.5(ITGB2):c.742-13G>A	rs5030670	0.12263
NM_000211.5(ITGB2):c.31C>T (p.Leu11=)	rs5030667	0.01960

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.