Annotation Detail
Information
- Associated Genes
- ZNF469
- Associated Variants
-
ZNF469 p.Leu3032_Thr3036del (p.L3032_T3036del)
(
ENST00000437464.1,
ENST00000565624.3 )
ZNF469 p.Leu3032_Thr3036del (p.L3032_T3036del) ( ENST00000437464.1, ENST00000565624.3 ) - Source Database
- ClinVar
- Description
- NM_001367624.2(ZNF469):c.9095_9109del (p.Leu3032_Thr3036del) AND Cardiovascular phenotype
- ClinVar Allele ID
- 132460
- ClinVar RefSeq Alternation Syntax
- NM_001367624.2:c.9095_9109del
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2019-03-22
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002371941
- Observed Origin Sample
- germline
Drugs