Annotation Detail
Information
- Associated Genes
- IFNK
- Associated Variants
-
rs3849942
rs3849942 - Associated Disease
- amyotrophic lateral sclerosis
- Source Database
- DisGeNET
- Description
- [The chromosome 9p21 locus is a major cause of familial ALS in the Finnish population. Our data suggest the presence of a founder mutation for chromosome 9p21-linked ALS. Furthermore, the overlap with the risk haplotype recently reported for frontotemporal]
- Pubmed
- 20801718
- Original source reporting the Gene Disease association
- GAD
- DisGENET score for the Gene Disease association
- 0.00473406395720406
- Year of publication
- 2010
Drugs