Variant · Snv
NR3C2 NM_000901.5(NR3C2):c.2800-17C>G
CI-VAR-00047173Explore in graph →NM_000901.5:c.2800-17C>GClinVar 256831 rs61763143
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
- 2026-09-24
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260929-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 256831 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Chronic lymphocytic leukemia/small lymphocytic lymphoma; Uveal melanoma; Sarcoma; Ovarian serous cystadenocarcinoma; Familial pancreatic carcinoma; Gastric cancer; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Lung cancer; Cervical cancer | germline | 5 | Feb 04, 2026 | clinvar |