List of variants in gene RASGRP2 reported as pathogenic for blood platelet 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: 5

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001098671.2(RASGRP2):c.1142C>T (p.Ser381Phe)	rs767965347
NM_001098671.2(RASGRP2):c.1479dup (p.Arg494fs)	rs774996406
NM_001098671.2(RASGRP2):c.337C>T (p.Arg113Ter)	rs1592384832
NM_001098671.2(RASGRP2):c.706C>T (p.Gln236Ter)	rs2135780423
NM_001098671.2(RASGRP2):c.742G>T (p.Gly248Trp)	rs587777529

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.