Annotation Detail
Information
- Associated Genes
- ZNF469
- Associated Variants
-
ZNF469 p.Pro826= (p.P826=)
(
ENST00000565624.3,
ENST00000437464.1 )
ZNF469 p.Pro826= (p.P826=) ( ENST00000437464.1, ENST00000565624.3 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_001367624.2(ZNF469):c.2478G>T (p.Pro826=) AND not provided
- ClinVar Allele ID
- 132433
- ClinVar RefSeq Alternation Syntax
- NM_001367624.2:c.2478G>T
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2022-11-28
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003764808
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs