Variant · Snv
DIS3L2 NM_152383.5(DIS3L2):c.2289+37G>A
CI-VAR-00199729Explore in graph →NM_152383.5:c.2289+37G>AClinVar 1250509 rs1814893
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 |
|---|---|---|---|---|---|---|---|---|
| 1250509 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Familial pancreatic carcinoma; Nonpapillary renal cell carcinoma; Ovarian cancer; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Acute myeloid leukemia; Germ cell tumor of testis; Lymphoma; Ovarian serous cystadenocarcinoma; Uterine carcinosarcoma; Thymoma; Cholangiocarcinoma | germline | 3 | Feb 24, 2019 | clinvar |