Variant · Snv
LIMS2 NM_001161403.3(LIMS2):c.803-8C>G
CI-VAR-00047058Explore in graph →NM_001161403.3:c.803-8C>GClinVar 260989 rs115961120
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 |
|---|---|---|---|---|---|---|---|---|
| 260989 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Autosomal recessive limb-girdle muscular dystrophy type 2W; Gastric cancer; Ovarian serous cystadenocarcinoma; Sarcoma; Lung cancer; Ovarian cancer; Lymphoma; Cervical cancer; Uterine corpus endometrial carcinoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Clear cell carcinoma of kidney; Uveal melanoma; Familial pancreatic carcinoma; Thymoma; Cholangiocarcinoma; Malignant tumor of esophagus; Germ cell tumor of testis | germline | 4 | Feb 04, 2026 | clinvar |