Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1805054
HTR6
0.708 0.200 1 19666020 synonymous variant C/T snv 0.15; 8.0E-06 0.16 17
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
rs2445142
HSPG2
0.925 0.120 1 21899250 intron variant G/A;C snv 2
rs7528545
PDE4B
0.925 0.120 1 66227081 intron variant T/C snv 0.62 2
rs783036
PDE4B
0.925 0.120 1 66365687 synonymous variant G/A snv 0.48 0.56 2
rs878949
HSPG2
0.925 0.120 1 21900598 intron variant T/C snv 0.52 2
rs3943552
GLI2
0.925 0.120 2 120824482 intron variant C/T snv 0.14 2
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs334558
LOC107986119 ; GSK3B
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs995922697
GPX1
0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs6438552
GSK3B
0.790 0.280 3 119912967 intron variant A/G snv 0.54 9
rs3755557
GSK3B ; LOC107986119
0.807 0.280 3 120096110 non coding transcript exon variant T/A snv 0.14 6
rs6805251
GSK3B
0.925 0.120 3 119841759 intron variant T/A;C snv 4
rs7620754
LOC107986115
0.925 0.120 3 114229128 intron variant T/C snv 0.24 2
rs905568
LOC107986115
0.925 0.120 3 114232449 non coding transcript exon variant C/A;G;T snv 2
rs9878473
GSK3B
0.925 0.120 3 119931941 intron variant T/C snv 0.54 2
rs7669317 0.925 0.120 4 105536173 downstream gene variant T/C snv 2.9E-02 2
rs4532
DRD1
0.827 0.160 5 175443147 5 prime UTR variant C/T snv 0.68 0.72 7
rs5326
DRD1
0.851 0.160 5 175443193 5 prime UTR variant C/T snv 0.15 6
rs265975 0.925 0.120 5 175435192 downstream gene variant C/T snv 0.43 2
rs37364
PRLR
0.925 0.120 5 35072278 intron variant T/G snv 0.34 2
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs953038635
SOD2
0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51