Variant · Deletion
ABCC9 NM_020297.4(ABCC9):c.4450-6_4450-5del
CI-VAR-00124498Explore in graph →NM_020297.4:c.4450-6_4450-5delClinVar 695803 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
- 2026-09-06
- 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 |
|---|---|---|---|---|---|---|---|---|
| 695803 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Dilated cardiomyopathy 1O; Hypertrichotic osteochondrodysplasia Cantu type; Intellectual disability and myopathy syndrome; Atrial fibrillation, familial, 12; Colon adenocarcinoma; Cardiovascular phenotype | germline | 6 | Nov 01, 2025 | clinvar |