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SNP information rs1635852

RS1635852

Normal allele: TT

Polymorphism rs1635852 is related to topics like this:

Lupus is it genetic

It is now well understood that lupus is caused by both environmental and genetic factors. At...


Research and publications:

  18535201   A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose.

  18694974   Predicting type 2 diabetes based on polymorphisms from genome-wide association studies: a population-based study

  18952825   Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis.

  19341491   Genome-based prediction of common diseases: methodological considerations for future research

  19474294   Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

  19592620   Examination of type 2 diabetes loci implicates CDKAL1 as a birth weight gene.

  19933996   Examination of all type 2 diabetes GWAS loci reveals HHEX-IDE as a locus influencing pediatric BMI.

  20581827   Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.

  20966902   Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women.

  21379322   Risk alleles for systemic lupus erythematosus in a large case-control collection and associations with clinical subphenotypes.

  21408207   Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.

  22216288   Extent of height variability explained by known height-associated genetic variants in an isolated population of the Adriatic coast of Croatia.

  23328127   Allele-specific transcriptional activity at type 2 diabetes-associated single nucleotide polymorphisms in regions of pancreatic islet open chromatin at the JAZF1 locus.

  23740937   A systemic sclerosis and systemic lupus erythematosus pan-meta-GWAS reveals new shared susceptibility loci.

  24843659   Insights into the genetic basis of type 2 diabetes.

  24982668   Estimating the predictive ability of genetic risk models in simulated data based on published results from genome-wide association studies.

  25239271   Fine mapping of type 2 diabetes susceptibility loci.

  25328554   Systemic Sclerosis is a Complex Disease Associated Mainly with Immune Regulatory and Inflammatory Genes.

  25658847   Do variants associated with susceptibility to pancreatic cancer and type 2 diabetes reciprocally affect risk?

  26106387   Pathogenesis of Systemic Sclerosis.

  26157023   Strategies for fine-mapping complex traits.

  27027517   General Framework for Meta-Analysis of Haplotype Association Tests.

  27752041   Interactome-transcriptome analysis discovers signatures complementary to GWAS Loci of Type 2 Diabetes.

  28379579   Discovery of novel heart rate-associated loci using the Exome Chip.

  35124268   Mendelian Randomization Analysis Reveals No Causal Relationship Between Nonalcoholic Fatty Liver Disease and Severe COVID-19.

  19096518   A novel association of HK1 with glycated hemoglobin in a nondiabetic population: a genome-wide assessment of 14,618 Women's Genome Health Study participants.

Crohn's disease genetic

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

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...

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