Disease: Major Depressive Disorder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9862857
LOC101927995 ; LOC105377013
0.851 0.040 3 30453840 regulatory region variant A/G;T snv 4
rs9825823
FHIT
0.851 0.080 3 61096480 intron variant T/C snv 0.47 5
rs9722
S100B
0.776 0.200 21 46599326 3 prime UTR variant G/A snv 0.16; 2.4E-05 0.21 9
rs946903
BCL9
0.882 0.040 1 147625465 3 prime UTR variant T/C snv 0.25 3
rs945032
BDKRB2
0.882 0.040 14 96204324 upstream gene variant T/C snv 0.78 5
rs9394309
FKBP5
0.851 0.040 6 35654004 intron variant G/A snv 0.74 4
rs9364726 0.882 0.040 6 164236705 intergenic variant A/G snv 6.5E-02 3
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9321987
UTRN
0.925 0.040 6 144709148 intron variant C/T snv 0.40 3
rs9296158
FKBP5 ; LOC112267956
0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs853679
ZSCAN31
0.851 0.160 6 28329086 intron variant C/A snv 0.20 4
rs821616
DISC1 ; TSNAX-DISC1
0.752 0.200 1 232008852 missense variant A/T snv 0.26 0.29 13
rs8150
AANAT ; RHBDF2
0.807 0.160 17 76470935 3 prime UTR variant G/A;C snv 6
rs806371
CNR1
0.882 0.040 6 88146644 intron variant T/G snv 0.18 4
rs806368
CNR1
0.752 0.280 6 88140381 3 prime UTR variant T/C snv 0.19 14
rs80278479
TFAP2D
0.925 0.040 6 50758466 intron variant C/G snv 3.0E-03 3
rs7997012
HTR2A
0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs7973260
KSR2
0.851 0.120 12 117937681 intron variant A/G snv 0.83 7
rs796590326
P2RX7 ; LOC105370032
0.851 0.200 12 121162449 missense variant GT/AC mnv 5
rs794727961
CACNA1C
0.851 0.080 12 2512979 missense variant G/A snv 5
rs7828021 0.925 0.040 8 49727454 intergenic variant C/G;T snv 3
rs782212
LOC105378797
0.925 0.040 1 72479983 intron variant C/T snv 0.34 2
rs78087832 0.925 0.040 2 224600060 intergenic variant C/T snv 2.4E-03 3
rs77945277
BAZ1A
0.925 0.040 14 34840969 intron variant A/G snv 4.9E-03 3
rs77826363 0.882 0.040 6 1128802 intergenic variant G/T snv 2.2E-02 3