Variant · Deletion
FANCB NM_001018113.3(FANCB):c.1327-3del
CI-VAR-00018129Explore in graph →NM_001018113.3:c.1327-3delClinVar 93468 rs202067682
Curated evidence
Evidence by cancer (0 items)
Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.
Data not yet available
No curated evidence item references this variant yet.
ClinVar
Clinical significance (1)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
clinvarProvenance
- Source
- NCBI ClinVar (variant_summary)
- Dataset
- ClinVar variant_summary
- Version
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 93468 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Fanconi anemia; Inborn genetic diseases; FANCB-related disorder; Colorectal cancer; Hereditary cancer-predisposing syndrome; Papillary renal cell carcinoma type 1; Familial cancer of breast; Malignant lymphoma, large B-cell, diffuse; Fanconi anemia complementation group B; Familial pancreatic carcinoma | germline | 9 | Feb 03, 2026 | clinvar |