Variant · Snv
UBIAD1 NM_013319.3(UBIAD1):c.*148A>G
CI-VAR-00049995Explore in graph →NM_013319.3:c.*148A>GClinVar 291872 rs11580061
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
- 2026-09-14
- Retrieved
- Sep 15, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260915-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 291872 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Schnyder crystalline corneal dystrophy; Familial pancreatic carcinoma; Nonpapillary renal cell carcinoma; Cervical cancer; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Lung cancer; Sarcoma; Gastric cancer; Cholangiocarcinoma; Acute myeloid leukemia | germline | 3 | Jan 12, 2018 | clinvar |