Variant · Snv
MMP13 NM_002427.4(MMP13):c.800-9C>T
CI-VAR-00052755Explore in graph →NM_002427.4:c.800-9C>TClinVar 301984 rs17860556
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 |
|---|---|---|---|---|---|---|---|---|
| 301984 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Spondyloepimetaphyseal dysplasia, Missouri type; Metaphyseal anadysplasia; Malignant lymphoma, large B-cell, diffuse; Thymoma; Cervical cancer | germline | 5 | Feb 01, 2026 | clinvar |