Disease: Mental disorders
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs2509843 11 98254676 intergenic variant A/C;G;T snv 2
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs11740562
ADAM19
5 157515277 intron variant A/G snv 7.1E-02 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12745968
DIPK1A
1 92936280 intron variant A/G snv 0.36 2
rs4356203
PIK3C2A
0.925 0.040 11 17138601 intron variant A/G snv 0.31 4
rs165940
LOC107986348 ; PDE4D
0.925 0.040 5 59383658 intron variant A/T snv 0.38 4
rs17645023 1.000 0.040 17 66920916 intergenic variant A/T snv 0.22 3
rs11789407
LOC105376249
9 118597268 intergenic variant C/A snv 0.44 2
rs3800373
LOC101929309 ; FKBP5
0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs781720548
CPNE1 ; RBM12
0.882 0.040 20 35652946 stop gained C/A snv 5
rs6994992
NRG1
0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs17075286 3 43189231 intergenic variant C/G snv 5.9E-02 2
rs2018368 11 10718819 intergenic variant C/G snv 0.59 2
rs12282742
SAA2-SAA4 ; SAA2
11 18244252 intron variant C/G;T snv 2
rs7065696
PHF8
X 53947621 intron variant C/G;T snv 2
rs10275045
MAD1L1
0.882 0.160 7 1881190 intron variant C/T snv 0.35 5
rs17746001 0.925 0.040 4 179734472 intergenic variant C/T snv 5.3E-02 4
rs1992045
LOC105375856 ; LINC01602
8 57928365 intron variant C/T snv 0.14 2
rs2155907 11 98223945 intergenic variant C/T snv 0.38 2
rs2841307 6 100308811 intergenic variant C/T snv 0.20 2
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237