Variant · Other
KLHL41 NM_006063.3(KLHL41):c.1111-21_1111-18del
CI-VAR-00200514Explore in graph →NM_006063.3:c.1111-21_1111-18delClinVar 1272895 rs143361344
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 |
|---|---|---|---|---|---|---|---|---|
| 1272895 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Nemaline myopathy 9; Familial pancreatic carcinoma; Nonpapillary renal cell carcinoma; Ovarian cancer; Uveal melanoma; Lymphoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma | germline | 3 | Feb 02, 2026 | clinvar |