Variant · Snv
LBR NM_002296.4(LBR):c.367-79A>G
CI-VAR-00198674Explore in graph →NM_002296.4:c.367-79A>GClinVar 1223266 rs116020594
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 |
|---|---|---|---|---|---|---|---|---|
| 1223266 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Malignant lymphoma, large B-cell, diffuse; Cholangiocarcinoma; Lung cancer; Acute myeloid leukemia; Cervical cancer; Sarcoma; Gastric cancer; Uterine carcinosarcoma; Thymoma | germline | 3 | May 19, 2019 | clinvar |