rs231779, CTLA4

N. diseases: 5
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.
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.827 0.160 2 203869764 intron variant C/T snv 0.41 0.030 1.000 3 2010 2018
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
839 0.827 0.160 2 203869764 intron variant C/T snv 0.41 0.010 1.000 1 2011 2011
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
1451 0.827 0.160 2 203869764 intron variant C/T snv 0.41 0.010 1.000 1 2011 2011
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.827 0.160 2 203869764 intron variant C/T snv 0.41 0.010 1.000 1 2011 2011
Unipolar Depression
CUI: C0041696
Disease: Unipolar Depression
225 0.827 0.160 2 203869764 intron variant C/T snv 0.41 0.010 1.000 1 2011 2011