Variant · Snv
ABCB7 NM_001271696.3(ABCB7):c.246+1G>A
CI-VAR-00033336Explore in graph →NM_001271696.3:c.246+1G>AClinVar 213973 rs61323727
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 |
|---|---|---|---|---|---|---|---|---|
| 213973 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | ABCB7-related disorder; Sarcoma; Gastric cancer; Lymphoma; Ovarian serous cystadenocarcinoma; Clear cell carcinoma of kidney; Colon adenocarcinoma; Thyroid cancer, nonmedullary, 1; Cholangiocarcinoma; Cervical cancer; Uveal melanoma; Colorectal cancer; Thymoma; Melanoma; Lung cancer; Ovarian cancer; Uterine corpus endometrial carcinoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Acute myeloid leukemia; Hepatocellular carcinoma; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Adrenocortical carcinoma, hereditary | germline | 6 | Feb 01, 2026 | clinvar |