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: rs9879992
rs9879992
0.882 0.120 3 119993874 intron variant A/G snv 0.28
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2019 2019
dbSNP: rs9879992
rs9879992
0.882 0.120 3 119993874 intron variant A/G snv 0.28
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2019 2019
dbSNP: rs9879992
rs9879992
0.882 0.120 3 119993874 intron variant A/G snv 0.28
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
Neoplasms; Stomatognathic Diseases 0.010 1.000 1 2019 2019
dbSNP: rs9879992
rs9879992
0.882 0.120 3 119993874 intron variant A/G snv 0.28
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
Neoplasms; Stomatognathic Diseases 0.010 1.000 1 2019 2019
dbSNP: rs9878473
rs9878473
0.925 0.120 3 119931941 intron variant T/C snv 0.54
CUI: C3714760
Disease: Drug-induced tardive dyskinesia
Drug-induced tardive dyskinesia
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Chemically-Induced Disorders 0.010 1.000 1 2010 2010
dbSNP: rs9878473
rs9878473
0.925 0.120 3 119931941 intron variant T/C snv 0.54
CUI: C0686347
Disease: Tardive Dyskinesia
Tardive Dyskinesia
Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs7431209
rs7431209
1.000 0.040 3 119922595 intron variant A/G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs6808874
rs6808874
1.000 0.040 3 119839004 intron variant A/T snv 0.24
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
Mental Disorders 0.010 1.000 1 2008 2008
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: 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: rs6805251
rs6805251
0.925 0.120 3 119841759 intron variant T/A;C snv
CUI: C0686347
Disease: Tardive Dyskinesia
Tardive Dyskinesia
Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs6805251
rs6805251
0.925 0.120 3 119841759 intron variant T/A;C snv
CUI: C3714760
Disease: Drug-induced tardive dyskinesia
Drug-induced tardive dyskinesia
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Chemically-Induced Disorders 0.010 1.000 1 2010 2010
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: rs6779828
rs6779828
0.925 0.120 3 120056300 intron variant C/T snv 0.28
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2008 2008
dbSNP: rs6779828
rs6779828
0.925 0.120 3 120056300 intron variant C/T snv 0.28
CUI: C0392702
Disease: Abnormal involuntary movement
Abnormal involuntary movement
Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs6771023
rs6771023
0.882 0.040 3 119974764 intron variant T/C snv 0.22
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression
Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs6771023
rs6771023
0.882 0.040 3 119974764 intron variant T/C snv 0.22
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs6771023
rs6771023
0.882 0.040 3 119974764 intron variant T/C snv 0.22
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
Mental Disorders 0.010 1.000 1 2015 2015
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: 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: rs6438552
rs6438552
0.790 0.280 3 119912967 intron variant A/G snv 0.54
CUI: C3714760
Disease: Drug-induced tardive dyskinesia
Drug-induced tardive dyskinesia
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Chemically-Induced Disorders 0.010 1.000 1 2010 2010
dbSNP: rs6438552
rs6438552
0.790 0.280 3 119912967 intron variant A/G snv 0.54
CUI: C0040128
Disease: Thyroid Diseases
Thyroid Diseases
Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs6438552
rs6438552
0.790 0.280 3 119912967 intron variant A/G snv 0.54
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs6438552
rs6438552
0.790 0.280 3 119912967 intron variant A/G snv 0.54
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs6438552
rs6438552
0.790 0.280 3 119912967 intron variant A/G snv 0.54
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
Mental Disorders 0.010 1.000 1 2014 2014