ClinVar Miner

List of variants in gene ITGB2 reported as not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
Download table as spreadsheet
NM_000211.5(ITGB2):c.1062= (p.His354=) rs235330
NM_000211.5(ITGB2):c.1101C>A (p.Val367=) rs2230529
NM_000211.5(ITGB2):c.2147G>C (p.Gly716Ala) rs179363872
NM_000211.5(ITGB2):c.24G>T (p.Leu8=) rs11088969
NM_000211.5(ITGB2):c.382G>T (p.Asp128Tyr) rs137852615
NM_000211.5(ITGB2):c.500-11G>T rs55865320
NM_000211.5(ITGB2):c.58+12G>A rs2280965
NM_000211.5(ITGB2):c.715G>A (p.Ala239Thr) rs179363873
NM_000211.5(ITGB2):c.742-13G>A rs5030670
NM_000211.5(ITGB2):c.819G>A (p.Gly273=) rs2230528
NM_000211.5(ITGB2):c.899A>T (p.Asp300Val) rs179363874

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.