rs6779828, GSK3B

N. diseases: 2
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.
Abnormal involuntary movement
CUI: C0392702
Disease: Abnormal involuntary movement
10 0.925 0.120 3 120056300 intron variant C/T snv 0.28 0.010 1.000 1 2010 2010
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.925 0.120 3 120056300 intron variant C/T snv 0.28 0.010 1.000 1 2008 2008