Variant · Snv
CD33 NM_001772.4(CD33):c.924+2T>C
CI-VAR-00196417Explore in graph →NM_001772.4:c.924+2T>CClinVar 1164474 rs273621
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 |
|---|---|---|---|---|---|---|---|---|
| 1164474 | Benign | criteria provided, multiple submitters, no conflicts | 2 | CD33-related disorder; Sarcoma; Uterine corpus endometrial carcinoma; Cervical cancer; Gastric cancer; Thyroid cancer, nonmedullary, 1; Melanoma; Acute myeloid leukemia; Malignant tumor of esophagus | germline | 4 | Mar 30, 2023 | clinvar |