Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10011025
rs10011025
0.010 GeneticVariation BEFREE In this study, the association between the common rs10011025 variant in the GLRA3 locus, and albuminuria, was confirmed in 1259 independent Finnish individuals with type 1 diabetes (p = 0.0013), and meta-analysis of all Finnish individuals yielded a genome-wide significant association. 30120300

2018

dbSNP: rs1001179
rs1001179
CAT
0.020 GeneticVariation BEFREE There was no significant association between the CAT gene SNP rs1001179 and T1D or DPN. 29924645

2018

dbSNP: rs1001179
rs1001179
CAT
0.020 GeneticVariation BEFREE Major effects of two SNPs, C1167T (rs769217) and C(-262)T (rs1001179), of the catalase gene on T1D susceptibility have been reported previously in Russians from Moscow. 16453382

2006

dbSNP: rs1003878
rs1003878
0.700 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545

2007

dbSNP: rs1004446
rs1004446
C 0.810 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545

2007

dbSNP: rs1004446
rs1004446
C 0.810 GeneticVariation GWASCAT A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545

2007

dbSNP: rs1004446
rs1004446
0.810 GeneticVariation BEFREE Characteristics included are age at multiple autoantibody positivity, sex, selected high-risk HLA-DR-DQ genotypes, relationship to a family member with T1D, autoantibody at seroconversion, <i>INS</i> gene (rs1004446_A), and non-HLA gene polymorphisms identified by the Type 1 Diabetes Genetics Consortium (T1DGC). 28903990

2017

dbSNP: rs1004446
rs1004446
G 0.810 GeneticVariation GWASCAT Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases. 21829393

2011

dbSNP: rs1012411
rs1012411
0.700 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545

2007

dbSNP: rs1015166
rs1015166
T 0.800 GeneticVariation GWASCAT Genome wide identification of new genes and pathways in patients with both autoimmune thyroiditis and type 1 diabetes. 25936594

2015

dbSNP: rs1015166
rs1015166
0.800 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545

2007

dbSNP: rs10181656
rs10181656
0.010 GeneticVariation BEFREE The analysis of genotypes and haplotypes of the same SNPs (rs7574865, rs8179673, and rs10181656) showed very comparable degrees of risk for T1D. 19120275

2008

dbSNP: rs10186193
rs10186193
0.010 GeneticVariation BEFREE SNP rs10186193 (at RNASEH1 gene) showed association with T1D (P = 0.005). 29204916

2018

dbSNP: rs1020856343
rs1020856343
0.010 GeneticVariation BEFREE For these reasons, we investigated for the first time the association with T1D of six single nucleotide polymorphisms (SNPs) mapping to these candidate genes: slc2F2, slc2F11, T306I, L503F, OCTN2-promoter and OCTN2-intron. 16796743

2006

dbSNP: rs1022059218
rs1022059218
0.010 GeneticVariation BEFREE The 49A/G dimorphism in exon 1 and the (AT)n in the 3' untranslated region of the CTLA-4 gene were significantly associated with type 1 diabetes. 11685455

2001

dbSNP: rs1023934247
rs1023934247
0.010 GeneticVariation BEFREE Typing for HLA-DQA1 and DQB1 alleles showed that type 1 diabetes-predisposing DQ alpha/DQ beta heterodimers were less frequent in patients carrying N252S or P477A than in those carrying wild-type PRF1. 18198357

2008

dbSNP: rs10255021
rs10255021
0.700 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545

2007

dbSNP: rs10272724
rs10272724
0.010 GeneticVariation BEFREE The minor allele of rs10272724 (C) was found to be protective from type 1 diabetes (odds ratio 0.87 [95% CI 0.83-0.91]; P = 1.1 × 10(-11)). rs10272724 was not correlated with levels of two transcripts of IKZF1 in peripheral blood mononuclear cells. 21270240

2011

dbSNP: rs10277986
rs10277986
A 0.700 GeneticVariation GWASCAT Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers. 25751624

2015

dbSNP: rs10336
rs10336
0.010 GeneticVariation BEFREE A combination of a case (n = 447)-control (n = 300) and family (n = 221) analysis was performed to investigate the role of the CXCL9 (rs10336, rs3733236) and CXCL10 (rs3921, rs35795399 and rs8878) polymorphisms and their interaction with HLA high-risk haplotypes DQ2(DQA*0501-DQB*0201)-DQ8(DQA*0301-DQB*0302) in T1D. 19410617

2009

dbSNP: rs1041740
rs1041740
0.010 GeneticVariation BEFREE Further studies are necessary to assess the relationship between rs1041740 and T1D or DPN. 29924645

2018

dbSNP: rs1041981
rs1041981
0.700 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545

2007

dbSNP: rs1042713
rs1042713
0.010 GeneticVariation BEFREE We performed genotyping of the A265G (Arg16Gly) polymorphism in the ADRB2 gene in 85 patients with type 1 diabetes and classified them according to hypoglycemia awareness status. 18334922

2008

dbSNP: rs10484566
rs10484566
0.700 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545

2007

dbSNP: rs1048990
rs1048990
0.010 GeneticVariation BEFREE To fulfil this gap, single nucleotide polymorphisms in the PSMB5 (rs11543947), PSMA6 (rs2277460, rs1048990), PSMC6 (rs2295826, rs2295827) and PSMA3 (rs2348071) genes were genotyped on susceptibility to T1DM in Latvians. 26661414

2016