Variant · Snv
PLOD1 NM_000302.4(PLOD1):c.644-17T>G
CI-VAR-00055942Explore in graph →NM_000302.4:c.644-17T>GClinVar 384719 rs41307745
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 |
|---|---|---|---|---|---|---|---|---|
| 384719 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Ehlers-Danlos syndrome, kyphoscoliotic type 1; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Familial pancreatic carcinoma; Hepatocellular carcinoma; Ovarian cancer; Squamous cell carcinoma of the head and neck; Lymphoma; Uterine carcinosarcoma; Thymoma; Uterine corpus endometrial carcinoma; Uveal melanoma; Malignant lymphoma, large B-cell, diffuse; Cholangiocarcinoma; Nonpapillary renal cell carcinoma | germline | 9 | Feb 04, 2026 | clinvar |