Annotation Detail
Information
- Associated Genes
- IL17A
- Associated Variants
-
IL17A c.27+18G>A
(
ENST00000648244.1 )
IL17A c.27+18G>A ( ENST00000648244.1 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_002190.3(IL17A):c.27+18G>A AND not specified
- ClinVar Allele ID
- 1264989
- ClinVar RefSeq Alternation Syntax
- NM_002190.3:c.27+18G>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2024-01-24
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003487678
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs