Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs10947563
FKBP5
0.925 0.040 6 35685660 intron variant G/A snv 0.77 3
rs110402
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs11792633
IL33 ; LOC107987046
0.882 0.280 9 6248035 intron variant C/T snv 0.35 5
rs12701020
CRHR2
0.925 0.040 7 30655345 intron variant C/T snv 0.12 3
rs13438494
PCLO
1.000 0.040 7 82759398 intron variant T/G snv 0.61 6
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1800498
DRD2
0.882 0.080 11 113420866 intron variant G/A snv 0.44 4
rs1800532
TPH1
0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs1885884
HTR2A ; HTR2A-AS1
13 46856141 non coding transcript exon variant C/A;G;T snv 2
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs279826
GABRA2
1.000 0.080 4 46332192 intron variant A/G snv 0.46 4
rs279858
GABRA2
0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs3798347
FKBP5 ; LOC112267956
0.925 0.040 6 35633999 intron variant A/T snv 0.65 3
rs3804099
TLR2
0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs4537731 1.000 0.040 11 18047335 upstream gene variant T/C snv 0.48 3
rs4675690 2 207643083 intergenic variant C/T snv 0.48 3
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4722999
CRHR2
0.851 0.080 7 30654159 intron variant C/T snv 0.67 5
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs56372821
EPHX2 ; GULOP
1.000 0.080 8 27578983 intron variant G/A snv 0.13 2
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272