Annotation Detail
Information
- Associated Genes
- SLC22A4
- Associated Variants
-
SLC22A4 c.393+6607C>T
(
ENST00000200652.4 )
SLC22A4 c.393+6607C>T ( ENST00000200652.4 ) - Associated Disease
- rheumatoid arthritis
- Source Database
- ClinVar
- Description
- NM_003059.3(SLC22A4):c.393+6607C>T AND Rheumatoid arthritis
- ClinVar Allele ID
- 20788
- ClinVar RefSeq Alternation Syntax
- NM_003059.3:c.393+6607C>T
- Clinical Significance Description
- risk factor
- Clinical Significance Last Update
- 2003-12-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000006105
- ClinVar Disease
- Rheumatoid arthritis
- Observed Origin Sample
- germline
- Pubmed
- 14608356
Drugs