SNP information rs1077667
Normal allele: CC
LIGHT genetic variation is associated with susceptibility to multiple sclerosis.
Polymorphism rs1077667 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.
23037546 Serum levels of LIGHT in MS.
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.
30713765 Variants of Mitochondrial Genome and Risk of Multiple Sclerosis Development in Russians.
34353742 Genomic and functional evaluation of TNFSF14 in multiple sclerosis susceptibility.
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...