Annotation Detail
Information
- Associated Genes
- IFNL3 IFNL4
- Associated Variants
-
IFNL4 c.151-152G>A
(
ENST00000606380.2 )
IFNL4 c.151-152G>A ( ENST00000606380.2 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_001276254.2(IFNL4):c.151-152G>A AND not specified
- ClinVar Allele ID
- 227801
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-03-09
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000614473
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs