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SNP information rs102275

RS102275

Normal allele: CC

Polymorphism rs102275 is related to topics like this:

Crohn's disease genetic

A chronic disorder known as Crohn's disease is a multi-faceted condition that primarily impacts the...


Research and publications:

  19060906   Common variants at 30 loci contribute to polygenic dyslipidemia.

  19060910   Genome-wide association analysis of metabolic traits in a birth cohort from a founder population

  19750004   A systems genetics approach implicates USF1, FADS3, and other causal candidate genes for familial combined hyperlipidemia.

  19798445   Genetic determinants of circulating sphingolipid concentrations in European populations.

  20421590   Genetic causes of high and low serum HDL-cholesterol.

  21421807   Effects of 34 risk loci for type 2 diabetes or hyperglycemia on lipoprotein subclasses and their composition in 6,580 nondiabetic Finnish men

  21466885   Evaluation of the gene-age interactions in HDL cholesterol, LDL cholesterol, and triglyceride levels: the impact of the SORT1 polymorphism on LDL cholesterol levels is age dependent.

  21599946   The impact of FADS genetic variants on ω6 polyunsaturated fatty acid metabolism in African Americans.

  21733300   Differences in arachidonic acid levels and fatty acid desaturase (FADS) gene variants in African Americans and European Americans with diabetes or the metabolic syndrome.

  21810555   Genetic variation in base excision repair pathway genes, pesticide exposure, and prostate cancer risk.

  22073310   Association of genetic loci with blood lipids in the Chinese population.

  22359512   Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.

  22425169   Vitamin D dependent effects of APOA5 polymorphisms on HDL cholesterol.

  22544929   IRF5 risk polymorphisms contribute to interindividual variance in pattern recognition receptor-mediated cytokine secretion in human monocyte-derived cells.

  24956270   Large-scale East-Asian eQTL mapping reveals novel candidate genes for LD mapping and the genomic landscape of transcriptional effects of sequence variants.

  26374098   CPAG: software for leveraging pleiotropy in GWAS to reveal similarity between human traits links plasma fatty acids and intestinal inflammation.

  27015630   Insight into Genotype-Phenotype Associations through eQTL Mapping in Multiple Cell Types in Health and Immune-Mediated Disease.

  27132591   Integrative Multi-omic Analysis of Human Platelet eQTLs Reveals Alternative Start Site in Mitofusin 2.

  27317923   The 11th NORDIC NUTRITION CONFERENCE NNC2016.

  27766137   Epidemiology of colorectal cancer.

  29545352   Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms.

  30143393   Evidence for a potential role of miR-1908-5p and miR-3614-5p in autoimmune disease risk using integrative bioinformatics.

  31991592   Genome-Wide Association Study for Serum Omega-3 and Omega-6 Polyunsaturated Fatty Acids: Exploratory Analysis of the Sex-Specific Effects and Dietary Modulation in Mediterranean Subjects with Metabolic Syndrome.

  33193614   The Role of Genetically Determined Glycemic Traits in Breast Cancer: A Mendelian Randomization Study.

  21102463   Genome-wide meta-analysis increases the number of confirmed susceptibility loci for Crohn's disease to 71.

  27336838   Blood and gut eQTLs from an anti-TNF-resistant Crohn's disease cohort inform genetic association loci for IBD.

Is rheumatoid arthritis genetic

Chronic abnormal inflammation is the hallmark of rheumatoid arthritis, a disease that primarily...

Hereditary pancreatitis

Pancreatitis is a multifaceted ailment that can stem from various sources. If pancreatitis arises...

Heart attack genetic

Genetic predisposition, also referred to as familial predisposition, is a crucial risk factor for...

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