Disease: Depressive disorder
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
rs10223646
DSE
0.882 0.080 6 116296236 intron variant C/T snv 0.41 4
rs10410544
SIRT2
0.827 0.120 19 38894892 intron variant T/C snv 0.68 0.67 6
rs10514299
TMEM161B-AS1
0.827 0.120 5 88367793 intron variant C/T snv 0.21 6
rs10766075
ARNTL
0.925 0.080 11 13297040 intron variant C/T snv 0.27 6
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs10848635
CACNA1C
0.882 0.080 12 2207029 intron variant T/A;C snv 0.34 4
rs10997871
SIRT1
0.925 0.080 10 67913178 intron variant T/C snv 4.1E-03 3
rs11022778
ARNTL
0.925 0.080 11 13369313 intron variant T/A;G snv 6
rs11030104
BDNF ; BDNF-AS
0.790 0.240 11 27662970 intron variant A/G snv 0.16 12
rs1106634
ATP6V1B2
0.851 0.080 8 20208538 intron variant G/A;C;T snv 0.18 5
rs112025902 0.925 0.080 4 120232669 intron variant A/G;T snv 4
rs11636753
CHRNB4
0.882 0.120 15 78636604 intron variant G/T snv 0.35 4
rs11754661
MTHFD1L
0.851 0.120 6 150885942 intron variant G/A;T snv 6
rs11824092
ARNTL
0.925 0.080 11 13324747 intron variant T/C snv 0.62 7
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
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
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
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
rs139832701
CAV3
0.925 0.080 3 8773124 intron variant T/G snv 0.13 3