Variant · Snv
ABCA7 NM_019112.4(ABCA7):c.5570+5G>C
CI-VAR-00101033Explore in graph →NM_019112.4:c.5570+5G>CClinVar 546823 rs200538373
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 |
|---|---|---|---|---|---|---|---|---|
| 546823 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Alzheimer disease 9; ABCA7-related disorder; Sarcoma; Acute myeloid leukemia; Lung cancer; Cervical cancer | germline | 6 | Dec 16, 2024 | clinvar |