Disease: Depressive disorder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1432441
MAP2K1
0.882 0.040 15 66426943 intron variant G/A snv 0.27 3
rs1549854
MAP2K1
0.882 0.040 15 66404397 intron variant A/C;G snv 0.44 3
rs242939
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
0.882 0.120 17 45818213 intron variant C/T snv 0.86 3
rs10223646
DSE
0.882 0.080 6 116296236 intron variant C/T snv 0.41 4
rs1488864
LOC101927825 ; CAVIN3
0.851 0.080 11 6321099 intron variant T/G snv 0.80 4
rs1876828
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.851 0.160 17 45834159 intron variant C/T snv 0.14 4
rs760761
DTNBP1
0.882 0.080 6 15650901 intron variant G/A snv 0.26 4
rs1106634
ATP6V1B2
0.851 0.080 8 20208538 intron variant G/A;C;T snv 0.18 5
rs11904814
CREB1
0.851 0.080 2 207562074 intron variant T/G snv 0.30 5
rs12912233
RORA
0.851 0.120 15 60974897 intron variant C/T snv 0.38 5
rs174697
ARVCF ; COMT
0.851 0.080 22 19966309 intron variant A/G snv 0.88 5
rs4648308
PTGS2
0.851 0.160 1 186671485 downstream gene variant C/T snv 0.27 5
rs528732638
CHST9 ; AQP4-AS1
0.851 0.120 18 26940224 intron variant A/-;AA;AAA;AAAA delins 5
rs61888800
BDNF
0.851 0.080 11 27700731 5 prime UTR variant G/T snv 0.19 5
rs7296288
DHH
0.851 0.080 12 49086185 upstream gene variant A/C snv 0.50 5
rs766020740
MIR4761 ; COMT
0.851 0.120 22 19963644 missense variant C/A snv 4.0E-06 5
rs794727961
CACNA1C
0.851 0.080 12 2512979 missense variant G/A snv 5
rs9825823
FHIT
0.851 0.080 3 61096480 intron variant T/C snv 0.47 5
rs10514299
TMEM161B-AS1
0.827 0.120 5 88367793 intron variant C/T snv 0.21 6
rs1545843
LOC107984536
0.827 0.120 12 84170289 intron variant G/A snv 0.52 6
rs2253206 0.851 0.080 2 207527254 intron variant A/G snv 0.47 6
rs2619522
DTNBP1
0.827 0.080 6 15653418 intron variant A/C snv 0.26 6
rs28386840 0.827 0.080 16 55652906 upstream gene variant T/A;C snv 6
rs120074175
TPH2
0.827 0.080 12 72031544 missense variant G/A snv 1.2E-05 7.0E-06 7
rs1415125856
BDNF ; BDNF-AS
0.827 0.120 11 27658550 splice region variant G/A snv 4.0E-06 2.1E-05 7