Disease: Depressive disorder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10223646
DSE
0.882 0.080 6 116296236 intron variant C/T snv 0.41 4
rs10510057 0.925 0.080 10 119551536 intergenic variant G/C snv 0.22 3
rs10766075
ARNTL
0.925 0.080 11 13297040 intron variant C/T snv 0.27 6
rs1082214
MIP
0.925 0.080 12 56452706 non coding transcript exon variant C/T snv 9.3E-02 6
rs10848635
CACNA1C
0.882 0.080 12 2207029 intron variant T/A;C snv 0.34 4
rs10988134
KYAT1 ; SPOUT1
0.925 0.080 9 128833128 3 prime UTR variant C/T snv 0.34 4
rs10997871
SIRT1
0.925 0.080 10 67913178 intron variant T/C snv 4.1E-03 3
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
rs1106634
ATP6V1B2
0.851 0.080 8 20208538 intron variant G/A;C;T snv 0.18 5
rs11111
GDNF-AS1 ; GDNF
0.882 0.080 5 37814000 3 prime UTR variant T/C snv 0.22 5
rs112025902 0.925 0.080 4 120232669 intron variant A/G;T snv 4
rs115482041
RCL1
0.925 0.080 9 4860267 missense variant C/T snv 2.6E-03 2.3E-03 4
rs11824092
ARNTL
0.925 0.080 11 13324747 intron variant T/C snv 0.62 7
rs1187323
NTRK2
0.882 0.080 9 84668501 upstream gene variant C/A;G;T snv 5
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
rs120074175
TPH2
0.827 0.080 12 72031544 missense variant G/A snv 1.2E-05 7.0E-06 7
rs12137417
TSNAX-DISC1 ; DISC1
0.925 0.080 1 231950407 intron variant G/A snv 0.17 3
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
rs12936511
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
0.925 0.080 17 45807036 synonymous variant C/T snv 3.1E-02 3.0E-02 5
rs13440581
GPR50
0.882 0.080 X 151181399 missense variant A/G snv 0.45 0.45 5
rs1364647619
POMC
0.925 0.080 2 25161334 missense variant C/T snv 3