Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs762551
CYP1A2
0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs3730358
AKT1
0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs6438552
GSK3B
0.790 0.280 3 119912967 intron variant A/G snv 0.54 9
rs6805251
GSK3B
0.925 0.120 3 119841759 intron variant T/A;C snv 4
rs1338719
PDE4B
0.925 0.120 1 66183851 intron variant C/T snv 0.49 2
rs1890196
PDE4B
0.925 0.120 1 66337397 intron variant C/G;T snv 2
rs2015586
SLC18A2
0.925 0.120 10 117262226 intron variant C/T snv 0.58 2
rs2445142
HSPG2
0.925 0.120 1 21899250 intron variant G/A;C snv 2
rs363224
SLC18A2
0.925 0.120 10 117263062 intron variant C/A snv 0.48 2
rs37364
PRLR
0.925 0.120 5 35072278 intron variant T/G snv 0.34 2
rs3943552
GLI2
0.925 0.120 2 120824482 intron variant C/T snv 0.14 2
rs4739217
GFRA2
0.925 0.120 8 21727549 intron variant G/C snv 0.39 2
rs6587002
GFRA2
0.925 0.120 8 21723708 intron variant T/C;G snv 2
rs6988470
GFRA2
0.925 0.120 8 21742957 intron variant T/C snv 0.58 2
rs7528545
PDE4B
0.925 0.120 1 66227081 intron variant T/C snv 0.62 2
rs7620754
LOC107986115
0.925 0.120 3 114229128 intron variant T/C snv 0.24 2
rs878949
HSPG2
0.925 0.120 1 21900598 intron variant T/C snv 0.52 2
rs9878473
GSK3B
0.925 0.120 3 119931941 intron variant T/C snv 0.54 2
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1800566
NQO1
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57