Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs231775
rs231775
0.100 GeneticVariation BEFREE We performed case-control and family-based association studies to assess if the CTLA4 A49G and intron 1 C/T polymorphisms were associated with development of early onset type 1 diabetes in the Northern Ireland population. 11477480

2001

dbSNP: rs231775
rs231775
0.100 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: rs231775
rs231775
0.100 GeneticVariation BEFREE There was no evidence that the CTLA-4 exon 1 polymorphism (49 A/G) confers genetic susceptibility to type 1 diabetes mellitus in our case-control study in Japanese subjects. 10619986

1999

dbSNP: rs231775
rs231775
0.100 GeneticVariation BEFREE Our data indicate that CTLA-4 exon 1 position 49 A/G dimorphism was significantly associated with predisposition to IDDM in our Central Poland population, particularly in patients lacking the strongly predisposing DRB1 alleles. 9690057

1998

dbSNP: rs370443546
rs370443546
0.020 GeneticVariation BEFREE Studies on IDDM5 have led to the discovery of a novel polymorphism 163 A-->G (M55V) in SUMO4 gene, which was found to be associated with T1D patients with Asian origin. 17448564

2007

dbSNP: rs370443546
rs370443546
0.020 GeneticVariation BEFREE M55V variant of SUMO4 was significantly associated with type 1 diabetes in Asians, but genetic heterogeneity between Asian and Caucasian populations was suggested. 17130532

2006

dbSNP: rs5742909
rs5742909
0.010 GeneticVariation BEFREE Further subgroup analyses revealed that rs231775 polymorphism was significantly associated with susceptibility to T1DM in Caucasians and South Asians, and rs5742909 polymorphism was significantly associated with susceptibility to T1DM in South Asians. 30988065

2019