Variant · Deletion
ABCC9 NM_020297.4(ABCC9):c.4450-5del
CI-VAR-00006820Explore in graph →NM_020297.4:c.4450-5delClinVar 35634 rs4148680
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 |
|---|---|---|---|---|---|---|---|---|
| 35634 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Cardiomyopathy; Cardiovascular phenotype; Primary dilated cardiomyopathy; Dilated cardiomyopathy 1O; Hypertrophic cardiomyopathy 2; Familial cancer of breast | germline | 12 | Feb 03, 2026 | clinvar |