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SNP information rs3761959

RS3761959

Normal allele: CC

Polymorphism rs3761959 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:

  16859508   Association of the FCRL3 gene with rheumatoid arthritis: a further example of population specificity?

  17952073   Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants.

  18556175   Lack of association between Fc receptor-like 3 gene polymorphisms and systemic lupus erythematosus in Chinese population.

  19050767   Association between polymorphisms of FCRL3, a non-HLA gene, and Bechsche's disease in a Chinese population with ophthalmic manifestations.

  19452015   Polymorphisms of FCRL3 in a Chinese population with Vogt-Koyanagi-Harada (VKH) syndrome.

  20453842   Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.

  20626413   The association of Fc receptor-like 5 (FCRL5) with Graves' disease is secondary to the effect of FCRL3.

  22242199   Genetic factors of autoimmune thyroid diseases in Japanese.

  22355377   Caucasian and Asian specific rheumatoid arthritis risk loci reveal limited replication and apparent allelic heterogeneity in north Indians.

  22654555   Genetic basis of Graves' disease.

  23094030   Protein-protein interaction analysis highlights additional loci of interest for multiple sclerosis.

  24117236   The Fc receptor-like 3 gene polymorphisms and susceptibility to autoimmune diseases: an updated meta-analysis.

  25594855   FCRL3 gene polymorphisms confer autoimmunity risk for allergic rhinitis in a Chinese Han population.

  25829454   Novel Association Between Immune-Mediated Susceptibility Loci and Persistent Autoantibody Positivity in Type 1 Diabetes.

  25862376   Four FCRL3 Gene Polymorphisms (FCRL3_3, _5, _6, _8) Confer Susceptibility to Multiple Sclerosis: Results from a Case-Control Study.

  26051414   FCRL3 gene polymorphisms confer risk for sudden sensorineural hearing loss in a Chinese Han Population.

  26334889   Association of FCRL3 Genetic Polymorphisms With Endometriosis-Related Infertility Risk: An Independent Study in Han Chinese.

  26402798   The Fc Receptor-Like 3 Polymorphisms (rs7528684, rs945635, rs3761959 and rs2282284) and The Risk of Neuromyelitis Optica in A Chinese Population.

  27863461   Pooled genome-wide association reveals association upstream of FCRL3 with Graves' disease.

  31341856   Single nucleotide polymorphisms of FCRL3 in Iranian patients with Behçet's disease.

  31482761   Breakdown of multiple sclerosis genetics to identify an integrated disease network and potential variant mechanisms.

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