Annotation Detail
Information
- Associated Genes
- PLEKHG4B LOC123493256
- Associated Variants
-
GRCh38/hg38 5p15.33(chr5:22149-163286)x3
GRCh38/hg38 5p15.33(chr5:22149-163286)x3 - Source Database
- ClinVar
- Description
- GRCh38/hg38 5p15.33(chr5:22149-163286)x3 AND See cases
- ClinVar Allele ID
- 154631
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2010-11-30
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000134284
- Observed Origin Sample
- not provided
Drugs