Annotation Detail
Information
- Associated Genes
- MMP13 LOC126861318
- Associated Variants
-
NC_000011.10:g.102955810C>T
NC_000011.10:g.102955810C>T - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NC_000011.10:g.102955810C>T AND not provided
- ClinVar Allele ID
- 1156535
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2024-01-22
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001514053
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs