Annotation Detail
Information
- Associated Genes
- IL10RB IFNAR2-IL10RB
- Associated Variants
-
IFNAR2-IL10RB c.*85A>G, IL10RB c.*85A>G
(
ENST00000290200.7,
ENST00000609556.3,
ENST00000637650.2,
ENST00000433395.7 )
IFNAR2-IL10RB c.*85A>G, IL10RB c.*85A>G ( ENST00000290200.7, ENST00000609556.3, ENST00000637650.2, ENST00000433395.7 ) - Associated Disease
- inflammatory bowel disease 25
- Source Database
- ClinVar
- Description
- NM_000628.5(IL10RB):c.*85A>G AND Inflammatory bowel disease 25
- ClinVar Allele ID
- 351592
- ClinVar RefSeq Alternation Syntax
- NM_000628.5:c.*85A>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-01-13
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000270142
- ClinVar Disease
- Inflammatory bowel disease 25
- Observed Origin Sample
- germline
Drugs