Variant · Snv
TGFBR2 NM_003242.6(TGFBR2):c.95-3C>A
CI-VAR-00059877Explore in graph →NM_003242.6:c.95-3C>AClinVar 408434 rs375330013
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 |
|---|---|---|---|---|---|---|---|---|
| 408434 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Familial thoracic aortic aneurysm and aortic dissection; Loeys-Dietz syndrome 2; Colorectal cancer, hereditary nonpolyposis, type 6; Malignant tumor of esophagus; Diabetic retinopathy | germline | 10 | Jan 24, 2026 | clinvar |