List of variants in gene GATA2 reported as likely benign for not provided

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: 28

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_032638.5(GATA2):c.564G>C (p.Thr188=)	rs34870876	0.04681
NM_032638.5(GATA2):c.1233G>A (p.Ala411=)	rs34172218	0.01909
NM_032638.5(GATA2):c.230-194del	rs147454351	0.01523
NM_032638.5(GATA2):c.1017+215C>T	rs55665236	0.01484
NM_032638.5(GATA2):c.1018-194C>T	rs140421363	0.00935
NM_032638.5(GATA2):c.481C>G (p.Pro161Ala)	rs34799090	0.00854
NM_032638.5(GATA2):c.871+442G>C	rs144923197	0.00604
NM_032638.5(GATA2):c.1143+193A>G	rs375115092	0.00450
NM_032638.5(GATA2):c.*199C>G	rs545460836	0.00433
NM_032638.5(GATA2):c.872-182C>G	rs577184018	0.00326
NM_032638.5(GATA2):c.*183C>T	rs45598538	0.00308
NM_032638.5(GATA2):c.66C>G (p.Pro22=)	rs113384352	0.00264
NM_032638.5(GATA2):c.-5C>G	rs374415484	0.00260
NM_032638.5(GATA2):c.229+38C>T	rs188629393	0.00119
NM_032638.5(GATA2):c.1416G>A (p.Pro472=)	rs376805544	0.00022
NM_032638.5(GATA2):c.42G>T (p.Pro14=)	rs372722885	0.00011
NM_032638.5(GATA2):c.229+15C>G	rs767013148	0.00008
NM_032638.5(GATA2):c.189C>T (p.Pro63=)	rs763735447	0.00007
NM_032638.5(GATA2):c.1143+9G>A	rs533617078	0.00004
NM_032638.5(GATA2):c.543G>A (p.Val181=)	rs547329727	0.00003
NM_032638.5(GATA2):c.63C>T (p.His21=)	rs535362527	0.00002
NM_032638.5(GATA2):c.1113C>T (p.Asn371=)	rs376003468	0.00001
NM_032638.5(GATA2):c.1143+13C>T	rs112111696	0.00001
NM_032638.5(GATA2):c.1185T>C (p.Thr395=)	rs771739064	0.00001
NM_032638.5(GATA2):c.582C>T (p.Ala194=)	rs748710414	0.00001
NM_032638.5(GATA2):c.*118C>T	rs184208259
NM_032638.5(GATA2):c.1035C>G (p.Ala345=)	rs371599112
NM_032638.5(GATA2):c.872-95C>G	rs55914222

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.