Annotation Detail
Information
- Associated Genes
- IL10 IL19
- Associated Variants
-
IL19 c.-149+2474T>C
(
ENST00000656872.2,
ENST00000659642.2,
ENST00000659997.3,
ENST00000664374.2,
ENST00000659065.2 )
IL19 c.-149+2474T>C ( ENST00000659065.2, ENST00000659642.2, ENST00000664374.2, ENST00000656872.2, ENST00000659997.3 ) - Associated Disease
- Leprosy, susceptibility to, 1
- Source Database
- ClinVar
- Description
- NM_153758.5(IL19):c.-149+2474T>C AND Leprosy, susceptibility to, 1
- ClinVar Allele ID
- 1708942
- ClinVar RefSeq Alternation Syntax
- NM_153758.5:c.-149+2474T>C
- ClinVar RefSeq Alternation Syntax
- NM_001393490.1:c.-149+2722T>C
- Clinical Significance Description
- Uncertain risk allele
- Clinical Significance Last Update
- 2022-06-10
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002291818
- ClinVar Disease
- Leprosy, susceptibility to, 1
- Observed Origin Sample
- inherited
Drugs