Variant · Snv
NFKBIA NM_020529.3(NFKBIA):c.548-3C>T
CI-VAR-00052496Explore in graph →NM_020529.3:c.548-3C>TClinVar 313112 rs2233418
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 |
|---|---|---|---|---|---|---|---|---|
| 313112 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Ectodermal dysplasia and immunodeficiency 2; Sarcoma; Ovarian serous cystadenocarcinoma; Lung cancer; Familial cancer of breast; Gastric cancer; Uterine carcinosarcoma; Adrenocortical carcinoma, hereditary; Cervical cancer; Melanoma; Acute myeloid leukemia; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney; Colon adenocarcinoma; Colorectal cancer | germline | 8 | Jun 01, 2026 | clinvar |