Annotation Detail
Information
- Associated Genes
- ACTN3 BBS1 SLC29A2 RBM4 SPTBN2 CTSF RIN1 CCS DPP3 RBM14 YIF1A B4GAT1 BRMS1 CCDC87 PACS1 CD248 KLC2 MRPL11 TOP6BL RAB1B RBM4B PELI3 CNIH2 ZDHHC24 TMEM151A NPAS4 RBM14-RBM4
- Associated Variants
- GRCh37/hg19 11q13.2(chr11:65963737-66581485)x1
- Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- GRCh37/hg19 11q13.2(chr11:65963737-66581485)x1 AND not provided
- ClinVar Allele ID
- 1331787
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2021-05-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001827874
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs