Variant · Deletion
WDR19 NM_025132.4(WDR19):c.1480-3del
CI-VAR-00134838Explore in graph →NM_025132.4:c.1480-3delClinVar 811534 rs748620855
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 |
|---|---|---|---|---|---|---|---|---|
| 811534 | Benign | criteria provided, single submitter | 1 | Cervical cancer; Familial prostate cancer; Glioma susceptibility 1; Gastric cancer; Uterine carcinosarcoma; Squamous cell lung carcinoma; Cholangiocarcinoma | germline | 5 | Nov 29, 2023 | clinvar |