Disease: Schizophrenia
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1076560
DRD2
0.776 0.120 11 113412966 intron variant C/A snv 0.16 11
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs1130214
AKT1
0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 12
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs1164376164
ABCB1
0.851 0.200 7 87601024 5 prime UTR variant A/G snv 6
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2007153
DBH
0.882 0.080 9 133638697 intron variant T/C snv 0.61 3
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2283123
DBH
0.882 0.080 9 133650175 intron variant C/G;T snv 3
rs2283265
DRD2
0.776 0.160 11 113414814 intron variant C/A snv 0.16 12
rs2424932
DNMT3B
0.827 0.200 20 32808730 3 prime UTR variant A/G;T snv 5
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs334558
LOC107986119 ; GSK3B
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4746720
SIRT1
0.790 0.320 10 67917073 3 prime UTR variant T/C snv 2.4E-02 7
rs4880213 0.827 0.160 9 137136549 upstream gene variant C/G;T snv 6
rs4919621
PITX3
0.851 0.080 10 102238914 intron variant A/T snv 0.66 4
rs4925114
RAI1
0.925 0.080 17 17807956 intron variant A/G snv 0.53 4
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41