Disease: Mental disorders
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10949808 7 156255955 intergenic variant T/G snv 0.45 2
rs4813376
RIN2
20 19870811 intron variant T/G snv 0.86 2
rs6627057 X 145059799 downstream gene variant T/G snv 0.16 2
rs7219021
TTLL6
0.925 0.040 17 48763179 intron variant T/G snv 0.26 4
rs802568
CNTNAP2
0.925 0.040 7 146262151 intron variant T/G snv 0.17 4
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs802524
CNTNAP2
7 146254550 intron variant T/C;G snv 2
rs12201676 0.925 0.040 6 89022382 regulatory region variant T/C snv 0.21 4
rs2023239
CNR1
0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
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
rs7248363
PGPEP1
19 18357076 intron variant T/C snv 0.74 2
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 9
rs12527359 6 89018502 intergenic variant T/A snv 0.23 2
rs4570625
TPH2
0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs4996815 13 105999312 intron variant G/T snv 0.61 2
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs1806864 9 87416754 regulatory region variant G/C snv 7.4E-02 2
rs7727102 5 4720472 intron variant G/C snv 0.32 2
rs1992044
LOC105375856 ; LINC01602
8 57928349 intron variant G/A;T snv 2
rs11789399
LOC105376249
0.882 0.040 9 118597008 intergenic variant G/A;C snv 5
rs2054399
KCNMB2-AS1 ; KCNMB2
0.925 0.040 3 178623794 intron variant G/A;C snv 4
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