Disease: Mental disorders
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7872515
SPTLC1
0.925 0.040 9 92060258 intron variant G/A snv 0.25 4
rs802524
CNTNAP2
7 146254550 intron variant T/C;G snv 2
rs802568
CNTNAP2
0.925 0.040 7 146262151 intron variant T/G snv 0.17 4
rs993804
RARB
3 25070680 intron variant C/T snv 0.75 2
rs1009080 1 29958713 intergenic variant G/A snv 0.54 2
rs10949808 7 156255955 intergenic variant T/G snv 0.45 2
rs11789399
LOC105376249
0.882 0.040 9 118597008 intergenic variant G/A;C snv 5
rs11789407
LOC105376249
9 118597268 intergenic variant C/A snv 0.44 2
rs12527359 6 89018502 intergenic variant T/A snv 0.23 2
rs17075286 3 43189231 intergenic variant C/G snv 5.9E-02 2
rs17645023 1.000 0.040 17 66920916 intergenic variant A/T snv 0.22 3
rs17746001 0.925 0.040 4 179734472 intergenic variant C/T snv 5.3E-02 4
rs2018368 11 10718819 intergenic variant C/G snv 0.59 2
rs2155907 11 98223945 intergenic variant C/T snv 0.38 2
rs2509843 11 98254676 intergenic variant A/C;G;T snv 2
rs2841307 6 100308811 intergenic variant C/T snv 0.20 2
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs4949526 1.000 0.040 1 29959372 intergenic variant T/C snv 0.54 3
rs12201676 0.925 0.040 6 89022382 regulatory region variant T/C snv 0.21 4
rs1806864 9 87416754 regulatory region variant G/C snv 7.4E-02 2
rs781720548
CPNE1 ; RBM12
0.882 0.040 20 35652946 stop gained C/A snv 5
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24