Variant · Snv
ATP8B1 NM_001374385.1(ATP8B1):c.3016-9C>A
CI-VAR-00054692Explore in graph →NM_001374385.1:c.3016-9C>AClinVar 327470 rs34729241
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 |
|---|---|---|---|---|---|---|---|---|
| 327470 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Progressive familial intrahepatic cholestasis type 1; Uterine corpus endometrial carcinoma; Gastric cancer; Acute myeloid leukemia; Lung cancer; Cervical cancer; Familial intrahepatic cholestasis | germline | 7 | Apr 14, 2026 | clinvar |