Annotation Detail
Information
- Associated Genes
- ACP5 CNN1 ELAVL3 EPOR PRKCSH ZNF69 RAB3D ECSIT ZNF823 RGL3 ELOF1 ZNF700 ZNF439 ODAD3 ZNF653 ZNF441 ZNF491 ZNF440 SWSAP1 CCDC159 ZNF433 ZNF627 ZNF763 TMEM205 ZNF878
- Associated Variants
- GRCh37/hg19 19p13.2(chr19:11445773-12160664)x3
- Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- GRCh37/hg19 19p13.2(chr19:11445773-12160664)x3 AND not provided
- ClinVar Allele ID
- 804274
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2018-06-29
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001007032
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs