rs6438552, GSK3B

N. diseases: 9
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.790 0.280 3 119912967 intron variant A/G snv 0.54 0.050 0.800 5 2005 2013
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.790 0.280 3 119912967 intron variant A/G snv 0.54 0.020 1.000 2 2013 2015
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.790 0.280 3 119912967 intron variant A/G snv 0.54 0.010 1.000 1 2019 2019
Drug-induced tardive dyskinesia
CUI: C3714760
Disease: Drug-induced tardive dyskinesia
67 0.790 0.280 3 119912967 intron variant A/G snv 0.54 0.010 1.000 1 2010 2010
Invasive aspergillosis
CUI: C0238013
Disease: Invasive aspergillosis
13 0.790 0.280 3 119912967 intron variant A/G snv 0.54 0.010 1 2010 2010
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
1451 0.790 0.280 3 119912967 intron variant A/G snv 0.54 0.010 1.000 1 2014 2014
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.790 0.280 3 119912967 intron variant A/G snv 0.54 0.010 1.000 1 2019 2019
Tardive Dyskinesia
CUI: C0686347
Disease: Tardive Dyskinesia
67 0.790 0.280 3 119912967 intron variant A/G snv 0.54 0.010 1.000 1 2010 2010
Thyroid Diseases
CUI: C0040128
Disease: Thyroid Diseases
26 0.790 0.280 3 119912967 intron variant A/G snv 0.54 0.010 1.000 1 2018 2018