Annotation Detail
Information
- Associated Genes
- IL17A
- Associated Variants
-
IL17A c.*1249C>T
(
ENST00000648244.1 )
IL17A c.*1249C>T ( ENST00000648244.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_002190.3(IL17A):c.*1249C>T AND not provided
- ClinVar Allele ID
- 1258952
- ClinVar RefSeq Alternation Syntax
- NM_002190.3:c.*1249C>T
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2020-02-18
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001686082
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs