Annotation Detail
Information
- Associated Genes
- PDCD1
- Associated Variants
-
PDCD1 c.627+189G>C
(
ENST00000334409.10 )
PDCD1 c.627+189G>C ( ENST00000334409.10 ) - Associated Disease
- Multiple sclerosis modifier of disease progression
- Source Database
- ClinVar
- Description
- NM_005018.3(PDCD1):c.627+189G>C AND Multiple sclerosis modifier of disease progression
- ClinVar Allele ID
- 24290
- ClinVar RefSeq Alternation Syntax
- NM_005018.3:c.627+189G>C
- Clinical Significance Description
- risk factor
- Clinical Significance Last Update
- 2005-07-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000009833
- ClinVar Disease
- Multiple sclerosis modifier of disease progression
- Observed Origin Sample
- germline
- Pubmed
- 15912506
- Pubmed
- 12402038
Drugs