Disease: Depressive disorder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1187329
NTRK2
0.925 0.080 9 84674365 intron variant A/G snv 0.52 3
rs11904814
CREB1
0.851 0.080 2 207562074 intron variant T/G snv 0.30 5
rs11911834
S100B
0.882 0.080 21 46602608 5 prime UTR variant G/A;T snv 4
rs11932595
CLOCK
0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs1202184
ABCB1
0.851 0.120 7 87584585 intron variant C/T snv 0.39 7
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1212171
NTRK2
0.851 0.120 9 84667612 upstream gene variant C/T snv 0.50 8
rs12137417
TSNAX-DISC1 ; DISC1
0.925 0.080 1 231950407 intron variant G/A snv 0.17 3
rs1220000453
ZFP91-CNTF ; CNTF
0.882 0.120 11 58624189 synonymous variant C/T snv 5
rs12229394
TPH2
0.925 0.080 12 71999134 intron variant G/A snv 0.29 3
rs12630592
GSK3B
0.851 0.080 3 120049399 intron variant G/A;T snv 5
rs12912233
RORA
0.851 0.120 15 60974897 intron variant C/T snv 0.38 5
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1364647619
POMC
0.925 0.080 2 25161334 missense variant C/T snv 3
rs139832701
CAV3
0.925 0.080 3 8773124 intron variant T/G snv 0.13 3
rs1402757753
P2RX2
0.882 0.080 12 132621913 missense variant G/A snv 7.0E-06 4
rs1409851868
EPHA3
0.882 0.080 3 89399325 missense variant A/G snv 6
rs1415259
NOS1AP ; LOC105371475
0.925 0.080 1 162115519 intron variant C/T snv 0.54 5
rs1491850 0.925 0.080 11 27728178 intron variant T/C snv 0.37 6
rs1491851 0.925 0.080 11 27731216 intron variant T/C;G snv 0.41 4
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1545843
LOC107984536
0.827 0.120 12 84170289 intron variant G/A snv 0.52 6
rs156243 0.925 0.080 6 104416939 intergenic variant G/A snv 0.65 6
rs165774
COMT
0.807 0.120 22 19965038 3 prime UTR variant G/A snv 0.27 11
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92