Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Diabetes Mellitus, Non-Insulin-Dependent
0.500 SusceptibilityMutation disease CLINVAR
Diabetes Mellitus, Non-Insulin-Dependent
0.500 Biomarker disease HPO
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease BEFREE Genome-wide association studies have identified common, novel type 2 diabetes susceptibility loci within the FTO, CDKAL1, CDKN2A/CDKN2B, IGF2BP2, HHEX/IDE, and SLC30A8 gene regions. 17804762 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease BEFREE SNPs in other genes such as rs7756992 in CDKAL1, rs10811661 in CDKN2B and rs13266634 in SLC30A8 showed nominal association with type 2 diabetes. rs7756992 in CDKAL1 and rs10811661 in CDKN2B were correlated with impaired pancreatic beta cell function as estimated by the homeostasis model assessment beta index (p = 0.023, p = 0.0083, respectively). 17928989 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease GWASCAT Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. 17463246 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease GWASDB A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. 17463248 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease GWASCAT A genome-wide association study identifies novel risk loci for type 2 diabetes. 17293876 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease GWASDB Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. 17463249 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease GWASDB Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. 17463246 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease GWASDB A genome-wide association study identifies novel risk loci for type 2 diabetes. 17293876 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease GWASCAT A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. 17463248 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease GWASCAT Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. 17463249 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease BEFREE With collaborators (FUSION and WTCCC/UKT2D), we identified and confirmed three loci associated with T2D-in a noncoding region near CDKN2A and CDKN2B, in an intron of IGF2BP2, and an intron of CDKAL1-and replicated associations near HHEX and in SLC30A8 found by a recent whole-genome association study. 17463246 2007
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease BEFREE Of European non-diabetic offspring of type 2 diabetes patients, 46% are homozygous carriers of the Arg325Trp polymorphism in ZnT-8, which is known to associate with type 2 diabetes. 18324385 2008
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease BEFREE The R325W (rs13266634) nonsynonymous polymorphism in the islet-specific zinc transporter protein gene, SLC30A8, has been reported to be associated with type 2 diabetes and possibly with a defect in insulin secretion. 18162509 2008
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease BEFREE Association of CDKAL1, IGF2BP2, CDKN2A/B, HHEX, SLC30A8, and KCNJ11 with susceptibility to type 2 diabetes in a Japanese population. 18162508 2008
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease BEFREE In conclusion, we have shown that SNPs in HHEX, CDKN2A/B, CDKAL1, KCNQ1 and SLC30A8 confer a risk of T2DM in the Korean population. 18991055 2008
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease BEFREE We replicated the association with type 2 diabetes for rs10811661 in the vicinity of CDKN2B (OR 1.20, 95% CI: 1.06-1.37, p=0.004), rs9939609 in FTO (OR 1.14, 95% CI: 1.04-1.25, p=0.006) and rs13266634 in SLC30A8 (OR 1.20, 95% CI: 1.09-1.33, p=3.9 x 10(-4)). 18437351 2008
Diabetes Mellitus, Non-Insulin-Dependent
0.500 Biomarker disease BEFREE In addition to TCF7L2, SLC30A8 and HHEX, initially identified by the French GWA scan, CDKAL1, IGFBP2 and CDKN2A/2B strongly associate with T2D in French individuals, and mostly in populations of Central European descent but not in Moroccan subjects. 18461161 2008
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease BEFREE A genome-wide association study in the French population has detected that novel single-nucleotide polymorphisms (SNPs) in the IDE-KIF11-HHEX gene locus and the SLC30A8 gene locus are associated with susceptibility to type 2 diabetes. 17971426 2008
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease BEFREE Our results provide evidence that SLC30A8 is a susceptible locus for type 2 diabetes in Chinese population, and its variant can influence insulin secretion. 18628523 2008
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease BEFREE The type 2 diabetes nonsynonymous single nucleotide polymorphism (SNP) affecting aa(325) lies within the region of highest ZnT8 autoantibody (ZnT8A) binding, prompting an investigation of its relationship to type 1 diabetes. 18591387 2008
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease BEFREE When combined, each additional risk allele from CDKAL1-rs9465871, CDKN2A/B-rs10811661, IGF2BP2-rs4402960, and SLC30A8-rs13266634 increased the risk for type 2 diabetes by 1.24-fold (P = 2.85 x 10(-7)) or for combined IFG/type 2 diabetes by 1.21-fold (P = 6.31 x 10(-11)). 18633108 2008
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease BEFREE Genome-wide association scans in type 2 diabetes (T2D) have identified a risk variant, rs13266634 (Arg325Trp), in SLC30A8 on chromosome 8. 18400535 2008
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease BEFREE In obese subjects, associations with T2D were detected with PPARG Pro12Ala (OR = 0.73, P = 0.004), ADIPOQ -11,377C>G (OR = 1.26, P = 0.02), ENPP1 K121Q (OR = 1.30, P = 0.003) and TCF7L2 rs7903146 (OR = 1.30, P = 1.1 x 10-4), and non-significant associations with HNF1A I27L (OR = 0.96, P = 0.53), GCK -30G>A (OR = 1.15, P = 0.12) and SLC30A8 R325W (OR = 0.95, P = 0.44). 18498634 2008