Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs6296
HTR1B ; LOC105377864
0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs334558
LOC107986119 ; GSK3B
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs7997012
HTR2A
0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs1187352
NTRK2
0.925 0.040 9 84678542 intron variant T/A;C snv 3
rs17710780 1.000 0.040 5 149657413 regulatory region variant T/C snv 9.8E-02 1
rs747762300
CSF2
1.000 0.040 5 132074826 missense variant A/C snv 4.0E-06 1
rs1928040
HTR2A
1.000 0.040 13 46873101 intron variant G/A snv 0.49 1
rs12729558
KYAT3
1.000 0.040 1 88937277 intron variant C/G;T snv 1