Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10078866
DRD1
1.000 0.080 5 175445317 upstream gene variant A/G snv 5.2E-02 2
rs10196867
CTNNA2
0.925 0.080 2 79751234 intron variant C/G;T snv 5
rs1022563
PDYN-AS1
0.925 0.080 20 1973693 intron variant C/G;T snv 2
rs1042114
OPRD1
0.807 0.120 1 28812463 missense variant G/C;T snv 0.91 6
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs10494334 1.000 0.080 1 163535374 intergenic variant G/A snv 0.10 1
rs1076560
DRD2
0.776 0.120 11 113412966 intron variant C/A snv 0.16 11
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs1079597
DRD2
0.827 0.080 11 113425564 intron variant C/T snv 0.18 5
rs11030096
BDNF-AS
0.925 0.160 11 27643996 intron variant T/A;C snv 3
rs11030104
BDNF ; BDNF-AS
0.790 0.240 11 27662970 intron variant A/G snv 0.16 12
rs1122079
RGS9
1.000 0.080 17 65218385 intron variant A/C;T snv 1
rs1137070
MAOA
0.763 0.160 X 43744144 synonymous variant T/C snv 0.62 9
rs11503014
GABRA2
1.000 0.080 4 46388848 5 prime UTR variant C/G snv 0.27 2
rs11606194
HTR3B
1.000 0.080 11 113910259 intron variant T/C snv 6.1E-02 1
rs1176744
HTR3B
0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs12364283
DRD2 ; LOC105369501
0.925 0.080 11 113476233 upstream gene variant A/G snv 5.8E-02 3
rs130058
HTR1B ; LOC105377864
0.790 0.120 6 77463564 5 prime UTR variant T/A;G snv 8
rs13306221
BDNF
0.851 0.120 11 27701142 intron variant C/T snv 5.9E-02 4
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1389752
MPDZ
0.925 0.080 9 13235288 intron variant A/G;T snv 2
rs147247472
AGBL4-IT1 ; AGBL4
0.925 0.080 1 49441901 intron variant G/A snv 7.3E-04 5
rs1530351
RGS9
0.925 0.080 17 65135491 intron variant G/A;C snv 2