Variant · Snv
CYP1B1 NM_000104.4(CYP1B1):c.-2G>A
CI-VAR-00050469Explore in graph →NM_000104.4:c.-2G>AClinVar 335958 rs9341245
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 |
|---|---|---|---|---|---|---|---|---|
| 335958 | Uncertain significance | criteria provided, multiple submitters, no conflicts | 2 | Irido-corneo-trabecular dysgenesis; Glaucoma 3A; Glaucoma 3, primary infantile, B; Anterior segment dysgenesis 6; Ovarian serous cystadenocarcinoma; Lymphoma; Ovarian cancer | germline | 4 | Apr 07, 2022 | clinvar |