Annotation Detail
Information
- Associated Genes
- SRSF8 ENDOD1 CWC15 KDM4D SESN3 KDM4E
- Associated Variants
- GRCh37/hg19 11q21(chr11:94681351-95176293)x1
- Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- GRCh37/hg19 11q21(chr11:94681351-95176293)x1 AND not provided
- ClinVar Allele ID
- 1332417
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2021-02-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001834496
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs