Variant · Snv
B3GALNT1 NM_003781.4(B3GALNT1):c.-27G>A
CI-VAR-00338936Explore in graph →NM_003781.4:c.-27G>AClinVar 3037666 rs2231256
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 |
|---|---|---|---|---|---|---|---|---|
| 3037666 | Benign | no assertion criteria provided | 0 | B3GALNT1-related disorder; Uterine corpus endometrial carcinoma; Gastric cancer; Nonpapillary renal cell carcinoma; Cervical cancer; Uterine carcinosarcoma; Thymoma; Thyroid cancer, nonmedullary, 1; Acute myeloid leukemia; Colon adenocarcinoma; Ovarian serous cystadenocarcinoma; Malignant tumor of esophagus; Lung cancer | germline | 2 | Oct 15, 2019 | clinvar |