Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1359790
rs1359790
LOC105370275
G 0.810 GeneticVariation GWASCAT Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls. 31118516

2019
dbSNP: rs1359790
rs1359790
LOC105370275
A 0.810 GeneticVariation GWASCAT Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes. 30054458

2018
dbSNP: rs1359790
rs1359790
LOC105370275
A 0.810 GeneticVariation GWASCAT Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease. 28869590

2017
dbSNP: rs1359790
rs1359790
LOC105370275
G 0.810 GeneticVariation GWASCAT Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. 22885922

2012
dbSNP: rs1359790
rs1359790
LOC105370275
0.810 GeneticVariation GWASDB Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. 22885922

2012
dbSNP: rs1359790
rs1359790
LOC105370275
0.810 GeneticVariation BEFREE The SNPs rs10906115 A and rs1359790 C are significantly associated with susceptibility to type 2 diabetes in the Japanese population, confirming that these alleles are common susceptibility variants for type 2 diabetes in East Asian populations. 21909839

2011
dbSNP: rs1359790
rs1359790
LOC105370275
G 0.810 GeneticVariation GWASDB Identification of new genetic risk variants for type 2 diabetes. 20862305

2010
dbSNP: rs1359790
rs1359790
LOC105370275
G 0.810 GeneticVariation GWASCAT Identification of new genetic risk variants for type 2 diabetes. 20862305

2010