Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13266634
rs13266634
SLC30A8 ; LOC105375716
T 1.000 SusceptibilityMutation CLINVAR

dbSNP: rs4402960
rs4402960
IGF2BP2
T 1.000 SusceptibilityMutation CLINVAR

dbSNP: rs12255372
rs12255372
TCF7L2
T 0.900 SusceptibilityMutation CLINVAR

dbSNP: rs11196205
rs11196205
TCF7L2
C 0.800 SusceptibilityMutation CLINVAR

dbSNP: rs137853240
rs137853240
HNF1A
A 0.800 SusceptibilityMutation CLINVAR

dbSNP: rs3792267
rs3792267
CAPN10
A 0.770 SusceptibilityMutation CLINVAR

dbSNP: rs137852783
rs137852783
PDX1
A 0.760 SusceptibilityMutation CLINVAR

dbSNP: rs2975760
rs2975760
CAPN10
C 0.730 SusceptibilityMutation CLINVAR

dbSNP: rs5030952
rs5030952
CAPN10
T 0.730 SusceptibilityMutation CLINVAR

dbSNP: rs137852786
rs137852786
PDX1
A 0.720 SusceptibilityMutation CLINVAR

dbSNP: rs3842570
rs3842570
CAPN10
AGATGATTCTGTCCCAGGAGCCGGGAGGAGGGT 0.720 SusceptibilityMutation CLINVAR

dbSNP: rs137852785
rs137852785
PDX1
C 0.710 SusceptibilityMutation CLINVAR

dbSNP: rs200998587
rs200998587
RBPJL
T 0.710 SusceptibilityMutation CLINVAR

dbSNP: rs2070895
rs2070895
LIPC ; ALDH1A2
A 0.710 SusceptibilityMutation CLINVAR

dbSNP: rs137852784
rs137852784
PDX1
T 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs141804752
rs141804752
MTNR1B
G 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs182349376
rs182349376
MTNR1B
T 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs184917682
rs184917682
MTNR1B
C 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs387906779
rs387906779
MTNR1B
C 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs76474829
rs76474829
LOC105372630
G 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs80356661
rs80356661
PDX1
T 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs13266634
rs13266634
SLC30A8 ; LOC105375716
C 1.000 GeneticVariation GWASCAT A genome-wide association study identifies novel risk loci for type 2 diabetes. 17293876

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

2007
dbSNP: rs13266634
rs13266634
SLC30A8 ; LOC105375716
1.000 GeneticVariation BEFREE In Chinese Han, we replicated the associations between 7 genetic loci and T2D, with risk allele-specific odds ratios (ORs) as follows: 1.27 (95% CI, 1.11-1.45; p = 0.0008) for CDKAL1-rs10946398, 1.26 (95% CI, 1.08-1.47; p = 0.003) for IGF2BP2-rs4402960, 1.19 (95% CI, 1.04-1.37; p = 0.009) for SLC30A8-rs13266634, 1.22 (95% CI, 1.06-1.41; p = 0.005) for CDKN2A/B-rs10811661, 1.20 (95% CI, 1.01-1.42; p = 0.03) for HHEX-rs5015480, 1.37 (95% CI, 1.19-1.69; p = 1.0 x 10(-4)) for KCNQ1-rs2237892, and 1.24 (95% CI, 1.01-1.52; p = 0.046) for FTO-rs8050136 after adjustment for age, gender, and body mass index. 20509872

2010
dbSNP: rs13266634
rs13266634
SLC30A8 ; LOC105375716
1.000 GeneticVariation 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