Annotation Detail
Information
- Associated Genes
- IL13
- Associated Variants
-
IL13 c.-93+487C>T
IL13 c.-93+487C>T - Associated Disease
- Inherited susceptibility to asthma
- Source Database
- ClinVar
- Description
- NM_001354991.2(IL13):c.-93+487C>T AND Inherited susceptibility to asthma
- ClinVar Allele ID
- 29711
- ClinVar RefSeq Alternation Syntax
- NM_001354991.2:c.-93+487C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354992.2:c.-220C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354993.2:c.-149C>T
- Clinical Significance Description
- risk factor
- Clinical Significance Last Update
- 2005-05-15
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000015784
- ClinVar Disease
- Inherited susceptibility to asthma
- Observed Origin Sample
- germline
- Pubmed
- 11588017
- Pubmed
- 15879126
- Pubmed
- 11709756
- Pubmed
- 12847555
Drugs