SNP information rs17066096
Normal allele: AA
A rare coding variant of the IL22RA2 signalling peptide is associated with multiple sclerosis risk.
Polymorphism rs17066096 is related to topics like this:
The presence of lesions on the brain and spinal cord is indicative of multiple sclerosis, a...
Research and publications:
22164203 Perspectives on the use of multiple sclerosis risk genes for prediction.
22396755 Genomic regions associated with multiple sclerosis are active in B cells.
23094030 Protein-protein interaction analysis highlights additional loci of interest for multiple sclerosis.
23730204 Progress in multiple sclerosis genetics.
27540591 Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies.
27802296 A Risk Score for Predicting Multiple Sclerosis.
27861577 Identifying Causal Genes at the Multiple Sclerosis Associated Region 6q23 Using Capture Hi-C.
31292217 IL-22 Binding Protein Promotes the Disease Process in Multiple Sclerosis.
Dementia is characterized as a syndrome, rather than a singular disease. Individuals with early...
Alzheimer's disease is a degenerative brain disease that causes dementia, resulting in a gradual...
Obsessive-compulsive disorder (OCD) is a mental health condition characterized by features known as...