Disease: Mental disorders
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
rs1009080 1 29958713 intergenic variant G/A snv 0.54 2
rs10275045
MAD1L1
0.882 0.160 7 1881190 intron variant C/T snv 0.35 5
rs10496702
NCKAP5
2 133247997 intron variant G/A snv 0.18 2
rs10949808 7 156255955 intergenic variant T/G snv 0.45 2
rs11164835
DIPK1A
1 92913536 intron variant G/A snv 0.35 2
rs11740562
ADAM19
5 157515277 intron variant A/G snv 7.1E-02 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
rs12201676 0.925 0.040 6 89022382 regulatory region variant T/C snv 0.21 4
rs12282742
SAA2-SAA4 ; SAA2
11 18244252 intron variant C/G;T snv 2
rs12527359 6 89018502 intergenic variant T/A snv 0.23 2
rs12745968
DIPK1A
1 92936280 intron variant A/G snv 0.36 2
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs165940
LOC107986348 ; PDE4D
0.925 0.040 5 59383658 intron variant A/T snv 0.38 4
rs17069122 6 108002555 downstream gene variant G/A snv 1.9E-02 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
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs17746001 0.925 0.040 4 179734472 intergenic variant C/T snv 5.3E-02 4
rs1806864 9 87416754 regulatory region variant G/C snv 7.4E-02 2
rs1992044
LOC105375856 ; LINC01602
8 57928349 intron variant G/A;T snv 2
rs1992045
LOC105375856 ; LINC01602
8 57928365 intron variant C/T snv 0.14 2
rs2018368 11 10718819 intergenic variant C/G snv 0.59 2