Disease: Depressive disorder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1043307
PSMD9
0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs1044396
CHRNA4
0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10997875 0.882 0.080 10 67920067 downstream gene variant T/A;C snv 4
rs11022778
ARNTL
0.925 0.080 11 13369313 intron variant T/A;G snv 6
rs112025902 0.925 0.080 4 120232669 intron variant A/G;T snv 4
rs1173546708
TPH1
0.851 0.120 11 18040661 synonymous variant G/A snv 4.0E-06 5
rs11754661
MTHFD1L
0.851 0.120 6 150885942 intron variant G/A;T snv 6
rs1187323
NTRK2
0.882 0.080 9 84668501 upstream gene variant C/A;G;T snv 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
rs1220000453
ZFP91-CNTF ; CNTF
0.882 0.120 11 58624189 synonymous variant C/T snv 5
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1232898090
PPARA
0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs12630592
GSK3B
0.851 0.080 3 120049399 intron variant G/A;T snv 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
rs1409851868
EPHA3
0.882 0.080 3 89399325 missense variant A/G snv 6
rs1417938
CRP
0.776 0.320 1 159714396 intron variant T/A;C snv 0.28 10
rs14259
PSMD9
0.724 0.360 12 121915890 missense variant A/C;G snv 4.0E-06; 0.32 19
rs143830698
ACE
0.882 0.120 17 63488659 missense variant G/A snv 8.4E-05 4
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs16139
NPY ; LOC107986777
0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs1718119
LOC105370032 ; P2RX7
0.689 0.520 12 121177300 missense variant G/A;T snv 0.35; 4.0E-06 21
rs1743963
SGK1
0.882 0.120 6 134176537 intron variant G/A;C snv 4