List of variants in gene WDR11 reported as pathogenic for autosomal recessive 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: 4

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_018117.12(WDR11):c.1255C>T (p.Gln419Ter)	rs2133748193
NM_018117.12(WDR11):c.1439del (p.Asn480fs)	rs747938475
NM_018117.12(WDR11):c.2931+1G>A	rs1252726486
NM_018117.12(WDR11):c.3033_3036del	rs760973100

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.