Variant · Deletion
GFM1 NM_024996.7(GFM1):c.1910-9_1910-8del
CI-VAR-00338873Explore in graph →NM_024996.7:c.1910-9_1910-8delClinVar 3043258 rs34920045
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 |
|---|---|---|---|---|---|---|---|---|
| 3043258 | Likely benign | criteria provided, single submitter | 1 | GFM1-related disorder; Colon adenocarcinoma; Malignant tumor of esophagus; Uterine corpus endometrial carcinoma; Colorectal cancer; Nonpapillary renal cell carcinoma | germline | 3 | Nov 25, 2024 | clinvar |