Disease: Unipolar Depression
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs10405744
ZNF93
0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 4
rs10494251
BCL9
0.851 0.040 1 147552120 intron variant C/T snv 5.8E-02 4
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs12649507
CLOCK
0.851 0.080 4 55514317 intron variant G/A;T snv 4
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs139459337
ZBTB20
0.882 0.040 3 114997018 intron variant C/T snv 4.7E-02 3
rs1541187
BCL9
0.882 0.040 1 147579693 intron variant C/G;T snv 3
rs16875288
ADAMTS16 ; LOC101929200
0.851 0.040 5 5297087 intron variant A/T snv 0.22 4
rs16935279
LINC01592
0.851 0.040 8 68961217 intron variant T/C snv 1.9E-02 4
rs17158930
DOCK4
0.851 0.040 7 111871082 intron variant A/G snv 0.25 4
rs17211233
RASGRF2
0.882 0.040 5 81072944 intron variant T/A;C snv 4
rs17673138
NRG1
0.851 0.040 8 32840440 intron variant A/C snv 8.6E-02 4
rs231779
CTLA4
0.827 0.160 2 203869764 intron variant C/T snv 0.41 5
rs4630333
TIMELESS
0.882 0.040 12 56443632 intron variant C/T snv 0.33 4
rs55945116
SEC11A
0.882 0.040 15 84676882 intron variant G/C snv 0.26 4
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs6586354 0.851 0.040 1 234897489 intron variant G/A snv 0.25 4
rs672607
BCL9
0.851 0.040 1 147581540 intron variant G/A snv 0.12 4
rs688325
BCL9
0.851 0.040 1 147605490 intron variant G/A snv 0.19 4
rs10968749
LINGO2
0.851 0.040 9 28752486 intergenic variant A/G snv 5.5E-02 4
rs11829119
LOC107984527
0.851 0.040 12 19040597 intergenic variant T/A;C snv 4
rs17154917 0.851 0.040 7 81207393 intergenic variant G/A;T snv 4
rs77826363 0.882 0.040 6 1128802 intergenic variant G/T snv 2.2E-02 3
rs9364726 0.882 0.040 6 164236705 intergenic variant A/G snv 6.5E-02 3