Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13266634
rs13266634
SLC30A8 ; LOC105375716
C 1.000 GeneticVariation GWASCAT Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. 17463246

2007
dbSNP: rs13266634
rs13266634
SLC30A8 ; LOC105375716
C 1.000 GeneticVariation GWASDB Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. 17463249

2007
dbSNP: rs13266634
rs13266634
SLC30A8 ; LOC105375716
C 1.000 GeneticVariation GWASDB A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. 17463248

2007
dbSNP: rs13266634
rs13266634
SLC30A8 ; LOC105375716
C 1.000 GeneticVariation GWASDB Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. 17463246

2007
dbSNP: rs13266634
rs13266634
SLC30A8 ; LOC105375716
1.000 GeneticVariation 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
dbSNP: rs13266634
rs13266634
SLC30A8 ; LOC105375716
C 1.000 GeneticVariation GWASCAT A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. 17463248

2007
dbSNP: rs13266634
rs13266634
SLC30A8 ; LOC105375716
T 1.000 SusceptibilityMutation CLINVAR