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SNP information rs3135338

RS3135338

Normal allele: TT

Polymorphism rs3135338 is related to topics like this:

Is multiple sclerosis hereditary disease

The presence of lesions on the brain and spinal cord is indicative of multiple sclerosis, a...

Research and publications:

  19143815   MHC fine mapping of human type 1 diabetes using the T1DGC data.

  20159113   Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene.

  21247752   Revealing the genetic basis of multiple sclerosis: are we there yet?

  23326239   A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1).

  24270849   Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data.

  29883771   20 μg hepatitis B vaccination reduced the risk of low responsiveness in infants with HLA-II risk genotype of HBsAg positive mothers.

  32568442   The genetic polymorphism down-regulating HLA-DRB1 enhancer activity facilitates HBV persistence, evolution and hepatocarcinogenesis in the Chinese Han population.

Dementia is genetic

Dementia is characterized as a syndrome, rather than a singular disease. Individuals with early...

Alzheimer's disease is hereditary

Alzheimer's disease is a degenerative brain disease that causes dementia, resulting in a gradual...

Is OCD obsessive compulsive disorder genetic

Obsessive-compulsive disorder (OCD) is a mental health condition characterized by features known as...

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