Annotation Detail
Information
- Associated Genes
- SLC22A5
- Associated Variants
-
SLC22A4 c.393+6607C>T
(
ENST00000200652.4 )
SLC22A4 c.393+6607C>T ( ENST00000200652.4 ) - Associated Disease
- Crohn Disease
- Source Database
- DisGeNET
- Description
- [Polymorphisms 3020insC in CARD15 and SNP rs3792876 in SLC22A4/5 occurred statistically significantly more often in patients with pediatric-onset CD than in patients with adult-onset CD. Polymorphisms 3020insC in CARD15 and SNP rs2165047 in DLG5 were assoc]
- Pubmed
- 17476680
- Original source reporting the Gene Disease association
- GAD
- DisGENET score for the Gene Disease association
- 0.0796694738711791
- Year of publication
- 2007
Drugs