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
rs1042173
SLC6A4
0.763 0.320 17 30197993 3 prime UTR variant A/C snv 0.40 14
rs1043307
PSMD9
0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs10510057 0.925 0.080 10 119551536 intergenic variant G/C snv 0.22 3
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
rs1082214
MIP
0.925 0.080 12 56452706 non coding transcript exon variant C/T snv 9.3E-02 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
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
rs11030101
BDNF-AS ; BDNF
0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36 10
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
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
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
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
rs1187323
NTRK2
0.882 0.080 9 84668501 upstream gene variant C/A;G;T snv 5