Variants in gene DDX41 with conflicting interpretations "risk factor" and "likely pathogenic"

Submission 1 (risk factor) minimum review status:		Submission 1 (risk factor) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely 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: 3

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_016222.4(DDX41):c.490C>T (p.Arg164Trp)	rs142143752	0.00017
NM_016222.4(DDX41):c.415_418dup (p.Asp140delinsGlyTer)	rs762890562	0.00007
NM_016222.4(DDX41):c.1187T>C (p.Ile396Thr)	rs747072227	0.00002

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.