Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs2023239
CNR1
0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs2283265
DRD2
0.776 0.160 11 113414814 intron variant C/A snv 0.16 12
rs2251214
SYT1
0.827 0.040 12 79430071 intron variant A/G;T snv 7
rs2070762
TH
0.925 0.080 11 2165105 intron variant A/G snv 0.43 5
rs678849
OPRD1
0.882 0.120 1 28818676 intron variant C/T snv 0.44 5
rs230530
NFKB1
0.882 0.080 4 102532823 intron variant A/G snv 0.37 4
rs4436578
DRD2
0.925 0.080 11 113436043 intron variant C/T snv 0.73 4
rs9444584
CNR1
0.882 0.160 6 88152840 intron variant C/T snv 0.30 4
rs1040288
NR3C2
1.000 0.040 4 148126966 intron variant G/C snv 0.49 3
rs11030096
BDNF-AS
0.925 0.160 11 27643996 intron variant T/A;C snv 3
rs604300
MGLL
1.000 0.080 3 127724009 intron variant A/G snv 0.91 3
rs9450898
CNR1
0.925 0.160 6 88154344 intron variant C/T snv 0.21 3
rs12043259
NFASC
1 204858913 intron variant C/G snv 0.11 2
rs1409568 1.000 0.040 10 118871273 intron variant T/C snv 8.2E-02 2
rs17664708
NRG1
1.000 0.080 8 32579499 intron variant C/T snv 1.0E-01 2
rs2377339
NCK2
2 105840835 intron variant A/G snv 4.8E-02 2
rs4648318
DRD2
1.000 0.080 11 113442667 intron variant T/C snv 0.33 2
rs2073837
DBH-AS1 ; DBH
9 133657806 intron variant G/A snv 0.31 1
rs382140 7 108141755 intergenic variant A/G snv 0.74 1
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
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