Variant · Snv
KDM5B NM_006618.5(KDM5B):c.2016+4A>G
CI-VAR-00127858Explore in graph →NM_006618.5:c.2016+4A>GClinVar 713774 rs61751237
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 |
|---|---|---|---|---|---|---|---|---|
| 713774 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Clear cell carcinoma of kidney; Acute myeloid leukemia; Adrenocortical carcinoma, hereditary; Colorectal cancer; Sarcoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Familial pancreatic carcinoma; Gastric cancer; Melanoma; Cholangiocarcinoma; Malignant tumor of esophagus; Lung cancer; Cervical cancer; Familial cancer of breast; Ovarian cancer | germline | 3 | Feb 01, 2026 | clinvar |