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
rs10968749
LINGO2
0.851 0.040 9 28752486 intergenic variant A/G snv 5.5E-02 4
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs11030101
BDNF-AS ; BDNF
0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36 10
rs11829119
LOC107984527
0.851 0.040 12 19040597 intergenic variant T/A;C snv 4
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
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
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
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
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
rs17066873 0.851 0.040 13 76889874 non coding transcript exon variant T/C snv 5.4E-02 4
rs17154917 0.851 0.040 7 81207393 intergenic variant G/A;T snv 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
rs17790731
RFESD
0.851 0.040 5 95647825 5 prime UTR variant C/T snv 4.9E-02 4
rs2137947
LOC105376934
0.882 0.040 3 4989276 downstream gene variant C/T snv 0.64 3
rs231779
CTLA4
0.827 0.160 2 203869764 intron variant C/T snv 0.41 5
rs334558
LOC107986119 ; GSK3B
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306