Annotation Detail
Information
- Associated Genes
- GCK
- Associated Variants
-
NC_000007.14:g.44189469C>T
NC_000007.14:g.44189469C>T - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NC_000007.14:g.44189469C>T AND not provided
- ClinVar Allele ID
- 1248234
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-06-28
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001671272
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs