Variant · Snv
ADAMTS10 NM_030957.4(ADAMTS10):c.1588-179G>T
CI-VAR-00197640Explore in graph →NM_030957.4:c.1588-179G>TClinVar 1188949 rs9749567
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 |
|---|---|---|---|---|---|---|---|---|
| 1188949 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Weill-Marchesani syndrome 1; Malignant lymphoma, large B-cell, diffuse | germline | 4 | Jul 14, 2021 | clinvar |