Annotation Detail
Information
- Associated Genes
- IFNL3
- Associated Variants
-
NC_000019.10:g.39252525T>G
NC_000019.10:g.39252525T>G - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NC_000019.10:g.39252525T>G AND not provided
- ClinVar Allele ID
- 227802
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-03-14
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000835188
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs