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SNP information rs3829251

RS3829251

Normal allele: GG

Associated with 25-hydroxyvitamin D levels.

Polymorphism rs3829251 is related to topics like this:

Genetic vitamin D deficiency

Vitamin D plays a vital role in maintaining musculoskeletal health. Recent studies have linked...


Research and publications:

  20418485   Genome-wide association study of circulating vitamin D levels.

  21828234   Common genetic variants in the vitamin D pathway including genome-wide associated variants are not associated with breast cancer risk among Chinese women

  21853245   The determinants of serum vitamin D levels in participants in a melanoma case-control study living in a temperate climate.

  21972121   Associations between common variants in GC and DHCR7/NADSYN1 and vitamin D concentration in Chinese Hans.

  22390397   Associations between polymorphisms related to calcium metabolism and human height: the Tromsø Study.

  22613962   Genetic influences on vitamin D status and forearm fracture risk in African American children.

  22649517   Polymorphisms related to the serum 25-hydroxyvitamin D level and risk of myocardial infarction, diabetes, cancer and mortality. The Tromsø Study.

  22740028   An exploratory analysis of common genetic variants in the vitamin D pathway including genome-wide associated variants in relation to glioma risk and outcome.

  22801813   The GC, CYP2R1 and DHCR7 genes are associated with vitamin D levels in northeastern Han Chinese children.

  24663808   A serum 25-hydroxyvitamin D concentration-associated genetic variant in DHCR7 interacts with type 2 diabetes status to influence subclinical atherosclerosis (measured by carotid intima-media thickness).

  25405862   Vitamin D insufficiency in Arabs and South Asians positively associates with polymorphisms in GC and CYP2R1 genes.

  26446360   Mendelian randomization studies of biomarkers and type 2 diabetes.

  26867646   Specific polymorphisms in the vitamin D metabolism pathway are not associated with susceptibility to Chlamydia trachomatis infection in humans.

  26959888   Germline genetics of cancer of unknown primary (CUP) and its specific subtypes.

  27652346   Mendelian randomization shows a causal effect of low vitamin D on multiple sclerosis risk.

  28423480   The effect of high-dose vitamin D supplementation on muscular function and quality of life in postmenopausal women-A randomized controlled trial.

  28703134   Genetic variants underlying vitamin D metabolism and VDR-TGFβ-1-SMAD3 interaction may impact on HCV progression: a study based on dbGaP data from the HALT-C study.

  29220424   Genetically deprived vitamin D exposure predisposes to atrial fibrillation.

  29291743   SNPs related to vitamin D and breast cancer risk: a case-control study.

  29476721   C3-epimerization of 25-hydroxyvitamin D increases with increasing serum 25-hydroxyvitamin D levels and shows a high degree of tracking over time.

  29761652   Vitamin D status and associated genetic polymorphisms in a cohort of UK children with non-alcoholic fatty liver disease.

  31959263   Vitamin D-related genes and cardiometabolic markers in healthy children: a Mendelian randomisation study.

  33553043   Vitamin D pathway-related gene polymorphisms and their association with metabolic diseases: A literature review.

  35115928   DBP rs7041 and DHCR7 rs3829251 are Linked to CD4(+) Recovery in HIV Patients on Antiretroviral Therapy.

  36012386   Vitamin D-Related Genetic Variations and Nonalcoholic Fatty Liver Disease: A Systematic Review.

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