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Type 1 diabetes is it genetic

diabetes1

By Li Dali, Ph.D.

If you tested your DNA with a personal genomics service like 23andMe, AncestryDNA, FamilyTreeDNA, MyHeritage or another testing company, you can learn more about your risk factors for hundreds of diseases. By clicking the button above ⬆️, you can upload your raw DNA data file and receive a personalized 250-page health report with research links that is the most comprehensive.

Our latest inclusion in the health report is the Type 1 Diabetes Genetic Risk Score, aimed at pinpointing individuals suitable for genetic testing for monogenic diabetes in cases where clinical features and autoimmune markers present ambiguity. This report offers autonomous insights for autoantibody and C-peptide testing, ensuring consistency as a DNA-based test, with results remaining constant over time.

Type 1 diabetes is a polygenic disease and common genetic variants have been identified that contribute to type 1 diabetes susceptibility. We genotype these variants and combine the risk of the individual variants that are present in a person to create a composite score that reflects an individual’s genetic susceptibility to type 1 diabetes.

On our website where you can easily upload raw DNA data file. This enables you to obtain a personalized health DNA report regarding T1D completely free of charge.

The likelihood of a patient having type 1 diabetes is based on the clinical information provided and the type 1 diabetes genetic risk score.

Follow the link of the selected polymorphism to read a brief description of how the selected polymorphism affects Type 1 diabetes and see a list of existing studies.

SNP polymorphisms related to the topic Type 1 diabetes:

rs6897932Variation in the IL7RA gene accounts for susceptibility to multiple sclerosis and type 1 diabetes.
rs725613Variation in the CLEC16A gene shows a consistent disease association with both multiple sclerosis and type 1 diabetes.
rs2476601This important SNP, located in the PTPN22 gene and also known as R620W or 1858C>T, may influence the risk of multiple autoimmune diseases such as rheumatoid arthritis, type 1 diabetes, autoimmune thyroiditis and systemic lupus erythematosus.
rs2292239The PTPN22 gene polymorphism associated with type 1 diabetes is related to the frequency of circulating regulatory T cells.
rs1893217The PTPN2 risk gene is associated with Crohn's disease and type 1 diabetes.
rs237025The gene for ubiquitin-like modifier 4 (SUMO4) predisposition to type 1 diabetes.
rs3087243The CTLA4 allelic variant alters T cell phosphorylation patterns and causes an increased risk of autoimmune diseases.
rs3772534SNP rs3772534 in the CBLB gene indicates an increased risk of developing type 1 diabetes.
rs763361rs763361, also known as Gly307Ser, is a SNP in the CD226 immune response gene. It is associated with an increased risk of multiple autoimmune diseases, including type 1 diabetes, multiple sclerosis, and rheumatoid arthritis.
rs3024505Predisposition variants for ulcerative colitis, Crohn's disease and type 1 diabetes.
rs12708716Polymorphisms influence the risk of developing type 1 diabetes.
rs45450798Polymorphisms affecting the disease process in type 1 diabetes and celiac disease.
rs3825932Polymorphism of susceptibility to type 1 diabetes and celiac disease.
rs4788084Polymorphism of increased risk of adult autoimmune diabetes and diabetic retinopathy.
rs2040410One of two polymorphisms (rs2040410 and rs7454108) that determine the highest risk of type 1 diabetes.
rs7454108One of two polymorphisms (rs2040410 and rs7454108) that determine the highest risk of type 1 diabetes.
rs11571316Influences predisposition to diabetes and progression from prediabetes to diabetes in at-risk individuals.
rs425105Increased risk of islet autoimmunity and type 1 diabetes.
rs478582Increased risk of islet autoimmunity and type 1 diabetes.
rs1465788Increased risk of islet autoimmunity and type 1 diabetes.
rs2664170Increased risk of islet autoimmunity and type 1 diabetes.
rs4763879Increased risk of islet autoimmunity and type 1 diabetes.
rs4900384Increased risk of islet autoimmunity and type 1 diabetes.
rs5753037Increased risk of islet autoimmunity and type 1 diabetes.
rs7202877Increased risk of islet autoimmunity and type 1 diabetes.
rs7804356Increased risk of islet autoimmunity and type 1 diabetes.
rs9388489Increased risk of islet autoimmunity and type 1 diabetes.
rs10517086Increased risk of islet autoimmunity and type 1 diabetes.
rs6441961Increased risk of gluten disease.
rs2069763Increased risk of autoimmune diseases - systemic lupus erythematosus, vasculitis, celiac disease, and newly diagnosed diabetes mellitus after transplantation.
rs2290400increased risk of autoimmune diabetes in adults.
rs11594656IL2RA gene polymorphism increases susceptibility to type I diabetes 1.19-fold for heterozygotes (AT) and 1.38-fold for homozygotes.
rs12722495IL2RA gene polymorphism associated with type 1 diabetes.
rs9272346HLA-DQA1 breakage is associated with a significant increase in risk (18-fold increase) of type 1 diabetes.
rs11171739Genetically dependent expression of ERBB3 modulates antigen-presenting cell function and risk of type 1 diabetes.
rs1701704Genetic variation associated with autoantibodies to insulin.
rs2816316Genetic variant risk for type 1 diabetes and gluten disease.
rs41295061Genetic predisposition to type 1 diabetes and autoimmune thyroiditis.
rs17388568Genetic predisposition to insulin-dependent type 1 diabetes.
rs11755527Genetic predisposition between three autoimmune diseases: rheumatoid arthritis, type 1 diabetes and gluten disease.
rs2104286Genetic heterogeneity of IL2RA indicates susceptibility to multiple sclerosis and susceptibility to type 1 diabetes.
rs1464510Common genetic variant in type 1 diabetes and celiac disease.
rs1738074Common genetic variant in type 1 diabetes and celiac disease.
rs17810546Common genetic variant in type 1 diabetes and celiac disease.
rs6822844Combined with the rs13119723 breakage, the study showed the strongest association with celiac disease among Caucasian patients.
rs1990760Associated with type 1 diabetes mellitus, organ-specific autoimmune diseases including Graves' disease.
rs6679677An allelic variant of the PHTF1 gene is associated with a 5.2-fold increased risk of type 1 diabetes and a 3.3-fold increased risk of rheumatoid arthritis.
rs3184504A variant of celiac disease genetic risk associated with immune response. Also carrier associated type 1 diabetes.
rs3788013A risk factor for islet autoimmunity and type 1 diabetes, as well as celiac disease, systemic lupus erythematosus and rheumatoid arthritis.
rs229541A predisposition locus for type 1 diabetes and celiac disease.
rs689A break in the INS insulin gene associated with the occurrence of type 1 and type 2 diabetes.
rs25421512-fold risk of developing Crohn's disease and 1.6-fold for type 1 diabetes.
rs176967361.94-fold risk of insulin-dependent type 1 diabetes.
rs75748651.3-fold risk of rheumatoid arthritis
rs757411
rs917997
rs947474
rs1004446
rs2069762
rs2296336
rs2544677
rs2639703
rs3129934
rs3741208
rs3746722
rs7528684
rs9811792
rs11052552
rs17166496

About The Author
Li Dali Li Dali

Li Dali, a National Foundation for Outstanding Youth Fund recipient, is a researcher at the School of Life Sciences in East China Normal University. He earned his PhD in genetics from Hunan Normal University in 2007 and conducted collaborative research at Texas A&M University during his doctoral studies. Li Dali and his team have optimized and innovated gene editing technology, leading to the establishment of a world-class system for constructing gene editing disease models.

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