Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4790953 0.851 0.160 17 65230912 downstream gene variant A/C snv 0.17 4
rs265975 0.925 0.120 5 175435192 downstream gene variant C/T snv 0.43 2
rs7669317 0.925 0.120 4 105536173 downstream gene variant T/C snv 2.9E-02 2
rs3730358
AKT1
0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1045280
ARRB2
0.882 0.160 17 4719343 synonymous variant C/T snv 0.71 0.62 3
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs1402139464
BDNF
0.882 0.160 11 27701009 5 prime UTR variant G/A;T snv 8.4E-06 3
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
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
rs762551
CYP1A2
0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs201934979
CYP1A2
0.882 0.160 15 74749838 missense variant C/T snv 8.8E-05; 8.0E-06 1.3E-04 3
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
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs6275
DRD2
0.851 0.160 11 113412755 synonymous variant A/G snv 0.64 0.58 7
rs767413934
DRD2
0.925 0.120 11 113424539 missense variant G/A snv 4.0E-06 2
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
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
rs3943552
GLI2
0.925 0.120 2 120824482 intron variant C/T snv 0.14 2