Variant · Snv
RFC2 NM_181471.3(RFC2):c.226-3C>T
CI-VAR-00306299Explore in graph →NM_181471.3:c.226-3C>TClinVar 2657587 rs41548312
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
- 2026-09-14
- Retrieved
- Sep 15, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260915-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 2657587 | Benign | criteria provided, single submitter | 1 | Chronic lymphocytic leukemia/small lymphocytic lymphoma; Uterine carcinosarcoma; Acute myeloid leukemia; Familial cancer of breast; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney; Ovarian serous cystadenocarcinoma; Melanoma; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Lung cancer; Cervical cancer; Colon adenocarcinoma; Sarcoma; Gastric cancer; Lymphoma | germline | 2 | Apr 01, 2026 | clinvar |