Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4532
DRD1
0.827 0.160 5 175443147 5 prime UTR variant C/T snv 0.68 0.72 7
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs762551
CYP1A2
0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs1045280
ARRB2
0.882 0.160 17 4719343 synonymous variant C/T snv 0.71 0.62 3
rs7528545
PDE4B
0.925 0.120 1 66227081 intron variant T/C snv 0.62 2
rs6275
DRD2
0.851 0.160 11 113412755 synonymous variant A/G snv 0.64 0.58 7
rs6988470
GFRA2
0.925 0.120 8 21742957 intron variant T/C snv 0.58 2
rs2015586
SLC18A2
0.925 0.120 10 117262226 intron variant C/T snv 0.58 2
rs783036
PDE4B
0.925 0.120 1 66365687 synonymous variant G/A snv 0.48 0.56 2
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs9878473
GSK3B
0.925 0.120 3 119931941 intron variant T/C snv 0.54 2
rs6438552
GSK3B
0.790 0.280 3 119912967 intron variant A/G snv 0.54 9
rs878949
HSPG2
0.925 0.120 1 21900598 intron variant T/C snv 0.52 2
rs334558
LOC107986119 ; GSK3B
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs1338719
PDE4B
0.925 0.120 1 66183851 intron variant C/T snv 0.49 2
rs363224
SLC18A2
0.925 0.120 10 117263062 intron variant C/A snv 0.48 2
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs265975 0.925 0.120 5 175435192 downstream gene variant C/T snv 0.43 2
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs4739217
GFRA2
0.925 0.120 8 21727549 intron variant G/C snv 0.39 2
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188