rs734312, WFS1

N. diseases: 10
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Mood Disorders
CUI: C0525045
Disease: Mood Disorders
0.030 GeneticVariation BEFREE The results of this meta-analysis suggest that there is no association between WFS1 gene H611R polymorphism and mood disorders. 25074416 2015
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
Mood Disorders
CUI: C0525045
Disease: Mood Disorders
0.030 GeneticVariation BEFREE If this finding will be replicated, the H611R polymorphism may be a possible marker for mood disorders in a psychiatric population, and not just in relatives of Wolfram syndrome probands. 19328217 2009
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
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
Mood Disorders
CUI: C0525045
Disease: Mood Disorders
0.030 GeneticVariation BEFREE Haplotype analysis revealed a common GTA haplotype, formed by SNPs 684C/G, 1185C/T and 1832G/A, conferring risk for affective disorders. 15473915 2005
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
0.020 GeneticVariation BEFREE The rs734312 from WFS1 gene was associated with diabetes at genotype level (P<0.01). 24477584 2014
Diabetes
CUI: C0011847
Disease: Diabetes
0.020 GeneticVariation BEFREE The rs734312 from WFS1 gene was associated with diabetes at genotype level (P<0.01). 24477584 2014
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
0.020 GeneticVariation BEFREE We genotyped the WFS1 SNPs rs10010131, rs752854 and rs734312 (H611R) in 3,548 DPP participants and performed Cox regression analysis using genotype, intervention and their interactions as predictors of diabetes incidence. 18060660 2008
Diabetes
CUI: C0011847
Disease: Diabetes
0.020 GeneticVariation BEFREE We genotyped the WFS1 SNPs rs10010131, rs752854 and rs734312 (H611R) in 3,548 DPP participants and performed Cox regression analysis using genotype, intervention and their interactions as predictors of diabetes incidence. 18060660 2008
Completed Suicide
CUI: C0852733
Disease: Completed Suicide
0.010 GeneticVariation BEFREE The nonsynonymous variants rs1383180 in EVC gene, rs6811863 in TBC1D1 gene, rs362272 in HTT gene, and rs734312 in WFS1 gene were associated to the male completed suicide. 19115052 2009
Suicidal
CUI: C0438696
Disease: Suicidal
0.010 GeneticVariation BEFREE The H611R polymorphism was associated with mood disorders but not suicidal behavior, aggressive/impulsive traits or suicidality in first-degree relatives. 19328217 2009
psychiatric hospitalization
CUI: C0748061
Disease: psychiatric hospitalization
0.010 GeneticVariation BEFREE Wolframin gene polymorphisms, including the H611R polymorphism, are reportedly associated with mood disorders and psychiatric hospitalization, but there is disagreement about the association of this specific variant with suicidality and impulsive traits. 19328217 2009
Analgesic Overuse Headache
CUI: C0522254
Disease: Analgesic Overuse Headache
0.010 GeneticVariation BEFREE To test the influence of WFS1 polymorphisms on medication overuse headache (MOH), a chronic headache condition related to symptomatic drugs overuse, we analyzed 82 MOH patients for the WFS1 His611Arg polymorphism, and performed a comparison between clinical features of Arg/Arg (R/R) and non-R/R individuals. 17719176 2007
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
0.010 GeneticVariation BEFREE None had the A559T and A602V mutations, and no association of G576S and H611R with bipolar disorder was found. 12565131 2003
Diabetes Mellitus, Insulin-Dependent
0.010 GeneticVariation BEFREE By genetic association studies of 185 type 1 diabetes patients and 380 control subjects, we found that R456H was significantly increased in the type 1 diabetes group compared to the control group (P = 0.0005); H611R and I720V were also significantly increased with weaker significance. 10679252 2000