Variants in gene CHD2 with conflicting interpretations "uncertain significance" and "pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 4

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001271.4(CHD2):c.1937G>A (p.Gly646Glu)	rs1567141162
NM_001271.4(CHD2):c.2705A>G (p.His902Arg)	rs2053935622
NM_001271.4(CHD2):c.3782G>T (p.Trp1261Leu)	rs1555444603
NM_001271.4(CHD2):c.4173del (p.Lys1391fs)	rs749969667

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.