ClinVar Miner

List of variants reported as likely benign for X-linked severe congenital neutropenia

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 9
Download table as spreadsheet
NM_000377.2(WAS):c.1255C>A (p.Leu419Met) rs1422863482
NM_000377.2(WAS):c.360+8A>G rs1557006508
NM_000377.2(WAS):c.391G>A (p.Glu131Lys) rs146220228
NM_000377.2(WAS):c.897G>A (p.Gly299=) rs782793103
NM_000377.3(WAS):c.1197A>G (p.Pro399=) rs1602179584
NM_000377.3(WAS):c.1253C>T (p.Ala418Val) rs781903491
NM_000377.3(WAS):c.141C>T (p.Ala47=) rs1602176588
NM_000377.3(WAS):c.339C>T (p.Phe113=) rs782233413
NM_000377.3(WAS):c.390C>T (p.Asp130=) rs782593697

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.