Annotation Detail
Information
- Associated Genes
- IL17F
- Associated Variants
-
IL17F p.His161Arg (p.H161R)
(
ENST00000336123.5,
ENST00000699946.1 )
IL17F p.His161Arg (p.H161R) ( ENST00000336123.5, ENST00000699946.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_052872.4(IL17F):c.482A>G (p.His161Arg) AND not provided
- ClinVar Allele ID
- 303622
- ClinVar RefSeq Alternation Syntax
- NM_052872.4:c.482A>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-11-12
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001618646
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs