Variant · Snv
WDR35 NM_020779.4(WDR35):c.2547+8T>A
CI-VAR-00362401Explore in graph →NM_020779.4:c.2547+8T>AClinVar 3585148
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 |
|---|---|---|---|---|---|---|---|---|
| 3585148 | Uncertain significance | criteria provided, single submitter | 1 | Short-rib thoracic dysplasia 7 with or without polydactyly; Cranioectodermal dysplasia 2; Malignant tumor of esophagus | germline | 2 | Jan 24, 2024 | clinvar |