Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10010131
rs10010131
Diabetes Mellitus, Non-Insulin-Dependent
0.060 GeneticVariation BEFREE All the risk alleles in the 11 examined type 2 diabetes risk variants showed an odds ratio (OR) greater than 1 for the GDM group compared with the control group ranging from 1.13 [95% confidence interval (CI) 0.88-1.46] to 1.44 (95% CI 1.19-1.74) except for the WFS1 rs10010131 variant with OR 0.87 (95% CI 0.73-1.05). 18984664

2009

dbSNP: rs10010131
rs10010131
Diabetes Mellitus, Non-Insulin-Dependent
0.060 GeneticVariation BEFREE A total of 1,578 non-diabetic individuals (534 men and 1,044 women, aged 40 +/- 13 years, BMI 28.9 +/- 8.2 kg/m(2) [mean +/- SD]) at increased risk of type 2 diabetes were genotyped for rs10010131 within the WFS1 gene. 19330314

2009

dbSNP: rs734312
rs734312
Diabetes Mellitus, Non-Insulin-Dependent
0.030 GeneticVariation BEFREE Our results suggested that the G allele of rs734312 polymorphism [dominant: FEM OR 0.873, 95%CI (0.810 - 0.940), recessive: FEM OR 0.876, 95% CI (0.800 - 0.959)] and A allele of rs10010131 polymorphism [dominant:FEM OR 0.853, 95% CI (0.817 - 0.892), recessive:REM OR 0.833, 95% CI (0.756 - 0.917)] in WFS1 gene had significant protective effects on risk of T2D. 23257691

2013

dbSNP: rs734312
rs734312
Diabetes Mellitus, Non-Insulin-Dependent
0.030 GeneticVariation BEFREE The WFS1 rs734312 showed a borderline significant association with type 2 diabetes with directions and relative risks consistent with previous reports. 18568334

2008

dbSNP: rs734312
rs734312
Diabetes Mellitus, Non-Insulin-Dependent
0.030 GeneticVariation BEFREE Four WFS1 SNPs (rs10010131, rs6446482, rs752854 and rs734312 [H611R]) were genotyped in a type 2 diabetes case-control study (n = 1,296/1,412) of Swedish adults. 18040659

2008

dbSNP: rs10012946
rs10012946
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE Examination of the publicly available Diabetes Genetics Initiative genome-wide association dataset revealed that rs10012946, which is in strong linkage disequilibrium with the three WFS1 SNPs (r(2)=0.88-1.0), was associated with type 2 diabetes (allelic odds ratio 0.85, 95% CI 0.75-0.97, p=0.026). 18060660

2008

dbSNP: rs3821943
rs3821943
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE HHEX, HMGA2, GLIS3, MTNR1B and PARK2) and some overlap with SNPs associated with T2D (e.g. rs3821943 near WFS1 and rs508419 near ANK1). 31123324

2019

dbSNP: rs4320200
rs4320200
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE The previously reported GWAS signal for T2D may be identified by the differential promoter activity of rs4320200, rs13107806, and rs13127445 in the promoter of WFS1 by nucleotide substitution. 25800097

2016

dbSNP: rs6446482
rs6446482
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE Not only did an association between WFS1-rs6446482 and early-onset T2D exist in the subgroup analysis, but TCF2-rs7501939 and WFS1-rs6446482 were also confirmed to confer risk for T2D in this meta-analysis. 20509872

2010

dbSNP: rs752854
rs752854
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE In the northern Swedish study, the minor allele at rs752854 was associated with reduced type 2 diabetes risk [odds ratio (OR) 0.85, 95% CI 0.75-0.96, p=0.010]. 18040659

2008