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SNP information rs703842

RS703842

Normal allele: GG

A gene associated with vitamin D, serum vitamin D concentration and risk of multiple sclerosis.

Polymorphism rs703842 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:

  16600026   Asthma families show transmission disequilibrium of gene variants in the vitamin D metabolism and signalling pathway

  18593774   Genetic and environmental determinants of 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D levels in Hispanic and African Americans

  18689381   Evidence for genetic regulation of vitamin D status in twins with multiple sclerosis.

  19255064   Vitamin D-related genes, serum vitamin D concentrations and prostate cancer risk

  19525955   Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20.

  20007432   Polymorphisms in vitamin D metabolism related genes and risk of multiple sclerosis

  20018050   Application of sex-specific single-nucleotide polymorphism filters in genome-wide association data.

  20186855   What role for genetics in the prediction of multiple sclerosis?

  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.

  20405052   The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.

  20648053   Confirmation of association between multiple sclerosis and CYP27B1.

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

  21358824   Prostate cancer susceptibility Loci identified on chromosome 12 in African Americans.

  21431378   Genetic predictors of 25-hydroxyvitamin D levels and risk of multiple sclerosis.

  21637794   Identification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissue.

  21852963   Pervasive sharing of genetic effects in autoimmune disease.

  22021740   Systematic review of genome-wide expression studies in multiple sclerosis.

  22190364   Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.

  22205958   Common variation in vitamin D pathway genes predicts circulating 25-hydroxyvitamin D Levels among African Americans.

  22357570   The Peru Urban versus Rural Asthma (PURA) Study: methods and baseline quality control data from a cross-sectional investigation into the prevalence, severity, genetics, immunology and environmental factors affecting asthma in adolescence in Peru

  23160276   Identification of a functional variant in the KIF5A-CYP27B1-METTL1-FAM119B locus associated with multiple sclerosis.

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

  23543094   Testing for associations between loci and environmental gradients using latent factor mixed models.

  23730204   Progress in multiple sclerosis genetics.

  25542806   Variants of CYP27B1 are associated with both multiple sclerosis and neuromyelitis optica patients in Han Chinese population.

  27175669   The Association Between Genetic Polymorphism rs703842 in CYP27B1 and Multiple Sclerosis: A Meta-Analysis.

  30361804   Replication study of GWAS risk loci in Greek multiple sclerosis patients.

  30875612   The association of rs703842 variants in CYP27B1 with multiple sclerosis susceptibility is influenced by the HLA-DRB1*15:01 allele in Slovaks.

  31398293   Contribution of CYP27B1 and CYP24A1 genetic variations to the incidence of acute coronary syndrome and to vitamin D serum level.

  32102946   Vitamin D Pathway and Other Related Polymorphisms and Risk of Prostate Cancer: Results from the Prostate Cancer Prevention Trial.

  32197412   Single Nucleotide Polymorphisms in 25-Hydroxyvitamin D3 1-Alpha-Hydroxylase (CYP27B1) Gene: The Risk of Malignant Tumors and Other Chronic Diseases.

  32518073   Multiple sclerosis risk variants regulate gene expression in innate and adaptive immune cells.

  32939414   Association of vitamin D gene polymorphisms in children with asthma - A systematic review.

  33484325   KIF5A and the contribution of susceptibility genotypes as a predictive biomarker for multiple sclerosis.

  34387450   [Association of vitamin D metabolism enzyme gene polymorphisms with multiple sclerosis risk: pilot study].

  35339045   Alterations of subset and cytokine profile of peripheral T helper cells in PBMCs from Multiple Sclerosis patients or from individuals with MS risk SNPs near genes CYP27B1 and CYP24A1.

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