Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13438494
PCLO
1.000 0.040 7 82759398 intron variant T/G snv 0.61 6
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs3804099
TLR2
0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs279858
GABRA2
0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs4537731 1.000 0.040 11 18047335 upstream gene variant T/C snv 0.48 3
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs698
ADH1C ; ADH1B
0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs9470080
FKBP5
0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs1800532
TPH1
0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs893290
RORA
15 61190958 intron variant G/T snv 0.96 1
rs110402
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs1800498
DRD2
0.882 0.080 11 113420866 intron variant G/A snv 0.44 4
rs10947563
FKBP5
0.925 0.040 6 35685660 intron variant G/A snv 0.77 3
rs56372821
EPHX2 ; GULOP
1.000 0.080 8 27578983 intron variant G/A snv 0.13 2
rs9316235
HTR2A
13 46871568 intron variant G/A snv 0.19 2
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
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs7044343
LOC107987046 ; IL33
0.752 0.520 9 6254208 intron variant C/T snv 0.51 13
rs11792633
IL33 ; LOC107987046
0.882 0.280 9 6248035 intron variant C/T snv 0.35 5
rs4722999
CRHR2
0.851 0.080 7 30654159 intron variant C/T snv 0.67 5
rs678849
OPRD1
0.882 0.120 1 28818676 intron variant C/T snv 0.44 5