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SNP information rs1004446

RS1004446

Normal allele: GG

Polymorphism rs1004446 is related to topics like this:

Type 1 diabetes is it genetic

Our latest inclusion in the health report is the Type 1 Diabetes Genetic Risk Score, aimed at...


Research and publications:

  17980034   Cubic exact solutions for estimating pairwise haplotype frequencies: Implications for linkage disequilibrium analysis and the CubeX web tool.

  18647951   A human type 1 diabetes susceptibility locus maps to chromosome 21q22.3.

  18840781   Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.

  19136655   Genome-wide scan for linkage to type 1 diabetes in 2,496 multiplex families from the Type 1 Diabetes Genetics Consortium.

  19732865   A generalized family-based association test for dichotomous traits.

  19956101   Overview of the Rapid Response data

  19956106   Analysis of 19 genes for association with type I diabetes in the Type I Diabetes Genetics Consortium families.

  20203524   Genetic susceptibility to type 2 diabetes is associated with reduced prostate cancer risk

  20639793   Association of birth weight with polymorphisms in the IGF2, H19, and IGF2R genes.

  21078522   Common genetic variation within IGFI, IGFII, IGFBP-1, and IGFBP-3 and endometrial cancer risk.

  21422097   Genetic variation in insulin-like growth factor 2 may play a role in ovarian cancer risk.

  21926269   Associations between paternally transmitted fetal IGF2 variants and maternal circulating glucose concentrations in pregnancy.

  21991322   Impact of the genome on the epigenome is manifested in DNA methylation patterns of imprinted regions in monozygotic and dizygotic twins.

  25117571   Circulating IGF1 and IGF2 and SNP genotypes in men and pregnant and non-pregnant women.

  25422107   Role of Type 1 Diabetes-Associated SNPs on Risk of Autoantibody Positivity in the TEDDY Study.

  25549360   Placental genome and maternal-placental genetic interactions: a genome-wide and candidate gene association study of placental abruption.

  26818947   Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes.

  27047537   Using Incomplete Trios to Boost Confidence in Family Based Association Studies.

  27331016   ERBB3-rs2292239 as primary type 1 diabetes association locus among non-HLA genes in Chinese.

  27716086   Association of CD247 (CD3ΞΆ) gene polymorphisms with T1D and AITD in the population of northern Sweden.

  28903990   The Influence of Type 1 Diabetes Genetic Susceptibility Regions, Age, Sex, and Family History on the Progression From Multiple Autoantibodies to Type 1 Diabetes: A TEDDY Study Report.

  32150081   Association of polymorphisms of preptin, irisin and adropin genes with susceptibility to coronary artery disease and hypertension.

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