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SNP information rs1111875

RS1111875

Normal allele: CC

HHEX gene polymorphism is associated with impaired proinsulin conversion and increased risk of developing type 2 diabetes.

Polymorphism rs1111875 is related to topics like this:

Type 2 diabetes genetic

Type 2 diabetes is the most prevalent and impactful subtype of diabetes worldwide, affecting around...

INSR Gene Insulin Receptor

The gene known as INSR directs the production of insulin receptors - proteins present in various...


Research and publications:

  17786204   Polymorphisms within novel risk loci for type 2 diabetes determine beta-cell function.

  17786212   Heterogeneity in meta-analyses of genome-wide association investigations

  17827400   Studies of association of variants near the HHEX, CDKN2A/B, and IGF2BP2 genes with type 2 diabetes and impaired insulin release in 10,705 Danish subjects: validation and extension of genome-wide association studies.

  17928989   Variations in the HHEX gene are associated with increased risk of type 2 diabetes in the Japanese population.

  17971426   Polymorphisms in the IDE-KIF11-HHEX gene locus are reproducibly associated with type 2 diabetes in a Japanese population.

  18039816   A candidate type 2 diabetes polymorphism near the HHEX locus affects acute glucose-stimulated insulin release in European populations: results from the EUGENE2 study.

  18162508   Association of CDKAL1, IGF2BP2, CDKN2A/B, HHEX, SLC30A8, and KCNJ11 with susceptibility to type 2 diabetes in a Japanese population

  18224312   Pharmacogenetics: data, concepts and tools to improve drug discovery and drug treatment

  18231124   HHEX gene polymorphisms are associated with type 2 diabetes in the Dutch Breda cohort.

  18264689   Polymorphisms in the TCF7L2, CDKAL1 and SLC30A8 genes are associated with impaired proinsulin conversion

  18423522   Estimating odds ratios in genome scans: an approximate conditional likelihood approach

  18426861   Association analysis of type 2 diabetes Loci in type 1 diabetes

  18437351   Genetic analysis of recently identified type 2 diabetes loci in 1,638 unselected patients with type 2 diabetes and 1,858 control participants from a Norwegian population-based cohort (the HUNT study)

  18443202   Association analysis in african americans of European-derived type 2 diabetes single nucleotide polymorphisms from whole-genome association studies

  18461161   Post genome-wide association studies of novel genes associated with type 2 diabetes show gene-gene interaction and high predictive value

  18469204   Implication of genetic variants near TCF7L2, SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, and FTO in type 2 diabetes and obesity in 6,719 Asians

  18477659   Replication of genome-wide association studies of type 2 diabetes susceptibility in Japan.

  18533027   Worldwide population differentiation at disease-associated SNPs

  18544707   Extension of type 2 diabetes genome-wide association scan results in the diabetes prevention program.

  18556337   Impact of diabetes susceptibility loci on progression from pre-diabetes to diabetes in at-risk individuals of the diabetes prevention trial-type 1 (DPT-1)

  18591388   Assessing the combined impact of 18 common genetic variants of modest effect sizes on type 2 diabetes risk

  18633108   Common variants in CDKAL1, CDKN2A/B, IGF2BP2, SLC30A8, and HHEX/IDE genes are associated with type 2 diabetes and impaired fasting glucose in a Chinese Han population.

  18689899   Exchangeable models of complex inherited diseases

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

  18782870   Clinical review: the genetics of type 2 diabetes: a realistic appraisal in 2008

  18852197   Metabolic and cardiovascular traits: an abundance of recently identified common genetic variants

  18991055   Association between polymorphisms in SLC30A8, HHEX, CDKN2A/B, IGF2BP2, FTO, WFS1, CDKAL1, KCNQ1 and type 2 diabetes in the Korean population.

  19001172   Analysis of the National Institute on Aging Family Study of Late-Onset Alzheimer's Disease: Impact of Additional Loci.

  19002430   Type 2 diabetes-associated genetic variants discovered in the recent genome-wide association studies are related to gestational diabetes mellitus in the Korean population

  19008344   Association analysis of variation in/near FTO, CDKAL1, SLC30A8, HHEX, EXT2, IGF2BP2, LOC387761, and CDKN2B with type 2 diabetes and related quantitative traits in Pima Indians

  19020323   Genotype score in addition to common risk factors for prediction of type 2 diabetes

  19033397   Replication study of candidate genes associated with type 2 diabetes based on genome-wide screening.

  19056611   Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data

  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.

  19117022   The influence of genetic variations in HHEX gene on insulin metabolism in the German MESYBEPO cohort.

  19161620   An open access database of genome-wide association results

  19228808   Type 2 diabetes risk alleles are associated with reduced size at birth.

  19258437   Genetic variant in the IGF2BP2 gene may interact with fetal malnutrition to affect glucose metabolism.

  19279076   Genetic predisposition, Western dietary pattern, and the risk of type 2 diabetes in men

  19324937   Previously associated type 2 diabetes variants may interact with physical activity to modify the risk of impaired glucose regulation and type 2 diabetes: a study of 16,003 Swedish adults

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

  19401414   Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population

  19455305   No association of multiple type 2 diabetes loci with type 1 diabetes

  19460916   Genetic architecture of type 2 diabetes: recent progress and clinical implications

  19502414   Association of 18 confirmed susceptibility loci for type 2 diabetes with indices of insulin release, proinsulin conversion, and insulin sensitivity in 5,327 nondiabetic Finnish men

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

  19615048   Type 2 diabetes gene TCF7L2 polymorphism is not associated with fetal and postnatal growth in two birth cohort studies.

  19626703   Were genome-wide linkage studies a waste of time? Exploiting candidate regions within genome-wide association studies

  19741467   Association of common type 2 diabetes risk gene variants and posttransplantation diabetes mellitus in renal allograft recipients in Korea.

  19794065   Polygenic risk variants for type 2 diabetes susceptibility modify age at diagnosis in monogenic HNF1A diabetes

  19808892   Combined risk allele score of eight type 2 diabetes genes is associated with reduced first-phase glucose-stimulated insulin secretion during hyperglycemic clamps

  19862325   PPARG, KCNJ11, CDKAL1, CDKN2A-CDKN2B, IDE-KIF11-HHEX, IGF2BP2 and SLC30A8 are associated with type 2 diabetes in a Chinese population

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

  19956539   How many genetic variants remain to be discovered?

  20017978   Influence of control selection in genome-wide association studies: the example of diabetes in the Framingham Heart Study

  20018041   The effect of multiple genetic variants in predicting the risk of type 2 diabetes

  20041287   Polymorphisms of TCF7L2 and HHEX genes in Chinese women with polycystic ovary syndrome.

  20043853   Prioritizing genes for follow-up from genome wide association studies using information on gene expression in tissues relevant for type 2 diabetes mellitus

  20049090   Association between type 2 diabetes loci and measures of fatness

  20075150   Utility of genetic and non-genetic risk factors in prediction of type 2 diabetes: Whitehall II prospective cohort study

  20080751   Long-range gene regulation links genomic type 2 diabetes and obesity risk regions to HHEX, SOX4, and IRX3.

  20126254   Rare variants create synthetic genome-wide associations.

  20142250   Diabetes genes and prostate cancer in the Atherosclerosis Risk in Communities study

  20144318   A strategy for analyzing gene-nutrient interactions in type 2 diabetes.

  20144327   A genomics study of type 2 diabetes mellitus in U.S. Air Force personnel

  20161779   Investigation of type 2 diabetes risk alleles support CDKN2A/B, CDKAL1, and TCF7L2 as susceptibility genes in a Han Chinese cohort

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

  20424228   Impact of common variants of PPARG, KCNJ11, TCF7L2, SLC30A8, HHEX, CDKN2A, IGF2BP2, and CDKAL1 on the risk of type 2 diabetes in 5,164 Indians.

  20490451   Type 2 diabetes risk alleles near ADCY5, CDKAL1 and HHEX-IDE are associated with reduced birthweight.

  20532014   The epidemiology of diabetes in Korea: from the economics to genetics.

  20550665   Association study of genetic variants in eight genes/loci with type 2 diabetes in a Han Chinese population.

  20647405   No association between FTO or HHEX and endometrial cancer risk.

  20712903   Obesity and diabetes genes are associated with being born small for gestational age: results from the Auckland Birthweight Collaborative study

  20865176   Consistent association of type 2 diabetes risk variants found in europeans in diverse racial and ethnic groups.

  20870969   Genetic predisposition to long-term nondiabetic deteriorations in glucose homeostasis: Ten-year follow-up of the GLACIER study

  20886378   Physiologic characterization of type 2 diabetes-related loci

  20929593   The longitudinal association of common susceptibility variants for type 2 diabetes and obesity with fasting glucose level and BMI.

  20979565   Population structure of Aggarwals of north India as revealed by molecular markers.

  20980412   Impact of positive family history and genetic risk variants on the incidence of diabetes: the Finnish Diabetes Prevention Study

  21056935   Quantitative assessment of the influence of hematopoietically expressed homeobox variant (rs1111875) on type 2 diabetes risk.

  21059810   Meta-analysis of the effect of HHEX gene polymorphism on the risk of type 2 diabetes.

  21084393   Type 2 diabetes (T2D) associated polymorphisms regulate expression of adjacent transcripts in transformed lymphocytes, adipose, and muscle from Caucasian and African-American subjects.

  21091714   The genetics of type 2 diabetes: what have we learned from GWAS?

  21103332   Combined effects of 19 common variations on type 2 diabetes in Chinese: results from two community-based studies

  21124985   Integrated genetic and epigenetic analysis identifies haplotype-specific methylation in the FTO type 2 diabetes and obesity susceptibility locus.

  21150882   Replication of genetic variants from genome-wide association studies with metabolic traits in an island population of the Adriatic coast of Croatia.

  21191145   Polymorphisms associated with type 2 diabetes in familial longevity: The Leiden Longevity Study.

  21278902   Genetic risk profiling for prediction of type 2 diabetes

  21283728   Genetic variants of diabetes risk and incident cardiovascular events in chronic coronary artery disease.

  21297524   The 1p13.3 LDL (C)-associated locus shows large effect sizes in young populations.

  21357383   No association of risk variants for diabetes and obesity with breast cancer: the Multiethnic Cohort and PAGE studies.

  21378175   Updated genetic score based on 34 confirmed type 2 diabetes Loci is associated with diabetes incidence and regression to normoglycemia in the diabetes prevention program

  21407270   Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration.

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

  21424820   Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration.

  21444075   Type 2 diabetes susceptibility single-nucleotide polymorphisms are not associated with polycystic ovary syndrome.

  21490949   Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia.

  21510814   Association of genetic variations in TCF7L2, SLC30A8, HHEX, LOC387761, and EXT2 with Type 2 diabetes mellitus in Tunisia.

  21533175   Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms.

  21565292   Random-effects model aimed at discovering associations in meta-analysis of genome-wide association studies.

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