Annotation Detail
Information
- Associated Genes
- IL17F
- Associated Variants
-
IL17F p.Glu126Gly (p.E126G)
(
ENST00000336123.5,
ENST00000699946.1 )
IL17F p.Glu126Gly (p.E126G) ( ENST00000336123.5, ENST00000699946.1 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_052872.4(IL17F):c.377A>G (p.Glu126Gly) AND not specified
- ClinVar Allele ID
- 303623
- ClinVar RefSeq Alternation Syntax
- NM_052872.4:c.377A>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2016-03-29
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000456093
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs