List of variants in gene ZNF469 reported as likely pathogenic 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: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001367624.2(ZNF469):c.19C>T (p.Arg7Ter)	rs1004428835	0.00037
NM_001367624.2(ZNF469):c.10324del (p.Arg3442fs)	rs756543273	0.00004
NM_001127464.2(ZNF469):c.1673del (p.Ala558Valfs)	rs1064795080
NM_001127464.2(ZNF469):c.3034delG (p.Val1012Serfs)	rs1555519050
NM_001127464.2(ZNF469):c.7554del (p.Ser2519Alafs)	rs886039575
NM_001367624.2(ZNF469):c.10332dup (p.Arg3445fs)	rs764470052
NM_001367624.2(ZNF469):c.11496_11505del (p.Ser3833fs)	rs1567517877
NM_001367624.2(ZNF469):c.2045_2063dup (p.Phe690fs)	rs2142300893
NM_001367624.2(ZNF469):c.2814del (p.Ser940fs)	rs1906051274
NM_001367624.2(ZNF469):c.2966_3012del (p.Arg989fs)	rs1906069048
NM_001367624.2(ZNF469):c.3754dup (p.Cys1252fs)	rs2142304720
NM_001367624.2(ZNF469):c.3959dup (p.Ala1321fs)	rs1906174955
NM_001367624.2(ZNF469):c.6444del (p.Gln2149fs)	rs886044697
NM_001367624.2(ZNF469):c.6664dup (p.Leu2222fs)	rs1361564558
NM_001367624.2(ZNF469):c.7860del (p.Val2621fs)

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.