Variant · Snv
WDR35 NM_020779.4(WDR35):c.1401-15T>G
CI-VAR-00232899Explore in graph →NM_020779.4:c.1401-15T>GClinVar 1581686 rs201903683
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 |
|---|---|---|---|---|---|---|---|---|
| 1581686 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Short-rib thoracic dysplasia 7 with or without polydactyly; Cranioectodermal dysplasia 2; Uterine corpus endometrial carcinoma | germline | 3 | Dec 03, 2025 | clinvar |