GSK3B, glycogen synthase kinase 3 beta, 2932

N. diseases: 393; N. variants: 25
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6805251
rs6805251
0.925 0.120 3 119841759 intron variant T/A;C snv
High density lipoprotein measurement
0.800 1.000 2 2013 2017
dbSNP: rs1154595
rs1154595
3 120017747 intron variant C/T snv 0.53
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs140442947
rs140442947
1.000 0.080 3 119865430 intron variant T/C snv 5.9E-03
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs16830551
rs16830551
3 119834031 intron variant C/T snv 2.4E-02
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs16830551
rs16830551
3 119834031 intron variant C/T snv 2.4E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs16830551
rs16830551
3 119834031 intron variant C/T snv 2.4E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs16830551
rs16830551
3 119834031 intron variant C/T snv 2.4E-02
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs1870931
rs1870931
3 120038166 intron variant C/G snv 0.24
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs6805251
rs6805251
0.925 0.120 3 119841759 intron variant T/A;C snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2013 2013
dbSNP: rs334558
rs334558
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.050 1.000 5 2009 2015
dbSNP: rs334558
rs334558
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.050 1.000 5 2011 2014
dbSNP: rs6438552
rs6438552
0.790 0.280 3 119912967 intron variant A/G snv 0.54
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.050 0.800 5 2005 2013
dbSNP: rs334558
rs334558
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
Mental Disorders 0.030 1.000 3 2014 2017
dbSNP: rs3755557
rs3755557
0.807 0.280 3 120096110 non coding transcript exon variant T/A snv 0.14
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.030 1.000 3 2011 2020
dbSNP: rs334558
rs334558
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.020 1.000 2 2013 2017
dbSNP: rs334558
rs334558
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
Mental Disorders 0.020 1.000 2 2012 2018
dbSNP: rs334558
rs334558
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
Mental Disorders 0.020 1.000 2 2008 2017
dbSNP: rs334558
rs334558
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression
Mental Disorders 0.020 1.000 2 2017 2019
dbSNP: rs334558
rs334558
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51
CUI: C0024517
Disease: Major depression, single episode
Major depression, single episode
Mental Disorders 0.020 1.000 2 2012 2018
dbSNP: rs6438552
rs6438552
0.790 0.280 3 119912967 intron variant A/G snv 0.54
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.020 1.000 2 2013 2015
dbSNP: rs6782799
rs6782799
1.000 0.040 3 119891946 intron variant C/T snv 0.54
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
Mental Disorders 0.020 1.000 2 2010 2010
dbSNP: rs1189501362
rs1189501362
0.882 0.120 3 119863583 missense variant G/A snv 7.0E-06
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2003 2003
dbSNP: rs1189501362
rs1189501362
0.882 0.120 3 119863583 missense variant G/A snv 7.0E-06
CUI: C0236642
Disease: Pick Disease of the Brain
Pick Disease of the Brain
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2003 2003
dbSNP: rs1189501362
rs1189501362
0.882 0.120 3 119863583 missense variant G/A snv 7.0E-06
CUI: C0949664
Disease: Tauopathies
Tauopathies
Nervous System Diseases 0.010 1.000 1 2003 2003
dbSNP: rs1189501362
rs1189501362
0.882 0.120 3 119863583 missense variant G/A snv 7.0E-06
CUI: C0338451
Disease: Frontotemporal dementia
Frontotemporal dementia
Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders 0.010 1.000 1 2003 2003