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SNP information rs12044852

RS12044852

Normal allele: CC

Polymorphism rs12044852 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:

  18650830   Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians.

  19010793   Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.

  19237575   The role of the CD58 locus in multiple sclerosis.

  19865102   Multiple sclerosis susceptibility alleles in African Americans.

  20007504   Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci.

  20362272   Evidence for polygenic susceptibility to multiple sclerosis--the shape of things to come.

  20368992   Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients.

  21362770   Association study of ITGAM, ITGAX, and CD58 autoimmune risk loci in systemic sclerosis: results from 2 large European Caucasian cohorts.

  22164203   Perspectives on the use of multiple sclerosis risk genes for prediction.

  22411505   Replication study of multiple sclerosis (MS) susceptibility alleles and correlation of DNA-variants with disease features in a cohort of Austrian MS patients.

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

  24205329   Detection of regulatory SNPs in human genome using ChIP-seq ENCODE data.

  28601281   Association of CD58 gene polymorphisms with NMO spectrum disorders in a Han Chinese population.

  31505972   Association of CD58 Polymorphisms and its Protein Expression with the Development and Prognosis of Autoimmune Thyroid Diseases.

  32257069   Association of CD58 polymorphism and multiple sclerosis in Malaysia: a pilot study.

  32760600   Association of rs12487066, rs12044852, rs10735781, rs3135388, rs6897932, rs1321172, rs10492972, and rs9657904 Polymorphisms with Multiple Sclerosis in Iranian 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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