Variant · Snv
CSF2RA NM_172245.4(CSF2RA):c.810+2T>A
CI-VAR-00210241Explore in graph →NM_172245.4:c.810+2T>AClinVar 1473649 rs2148504379
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 |
|---|---|---|---|---|---|---|---|---|
| 1473649 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Surfactant metabolism dysfunction, pulmonary, 4; CSF2RA-related disorder; Thyroid cancer, nonmedullary, 1 | germline | 4 | Nov 26, 2024 | clinvar |