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
rs334558
LOC107986119 ; GSK3B
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs2603751
NR4A1
0.925 0.120 12 52059498 3 prime UTR variant T/C snv 0.25 2
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
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
rs1402139464
BDNF
0.882 0.160 11 27701009 5 prime UTR variant G/A;T snv 8.4E-06 3
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs1805054
HTR6
0.708 0.200 1 19666020 synonymous variant C/T snv 0.15; 8.0E-06 0.16 17
rs76980269
NOS1
0.763 0.280 12 117330794 synonymous variant G/A snv 2.8E-05 4.2E-05 10
rs1806201
GRIN2B
0.776 0.200 12 13564574 synonymous variant G/A snv 0.32 0.24 8
rs6275
DRD2
0.851 0.160 11 113412755 synonymous variant A/G snv 0.64 0.58 7
rs1045280
ARRB2
0.882 0.160 17 4719343 synonymous variant C/T snv 0.71 0.62 3
rs2701124
NR4A1
0.925 0.120 12 52054373 synonymous variant G/A;C snv 9.5E-02 2
rs783036
PDE4B
0.925 0.120 1 66365687 synonymous variant G/A snv 0.48 0.56 2
rs3755557
GSK3B ; LOC107986119
0.807 0.280 3 120096110 non coding transcript exon variant T/A snv 0.14 6
rs905568
LOC107986115
0.925 0.120 3 114232449 non coding transcript exon variant C/A;G;T snv 2
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