Disease: Mental disorders
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7065696
PHF8
X 53947621 intron variant C/G;T snv 2
rs7248363
PGPEP1
19 18357076 intron variant T/C snv 0.74 2
rs7600871
NCKAP5
2 133257389 intron variant C/T snv 0.16 2
rs7727102 5 4720472 intron variant G/C snv 0.32 2
rs802524
CNTNAP2
7 146254550 intron variant T/C;G snv 2
rs993804
RARB
3 25070680 intron variant C/T snv 0.75 2
rs11789399
LOC105376249
0.882 0.040 9 118597008 intergenic variant G/A;C snv 5
rs12201676 0.925 0.040 6 89022382 regulatory region variant T/C snv 0.21 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
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
rs2054399
KCNMB2-AS1 ; KCNMB2
0.925 0.040 3 178623794 intron variant G/A;C snv 4
rs4356203
PIK3C2A
0.925 0.040 11 17138601 intron variant A/G snv 0.31 4
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
rs6484218
CAND1.11 ; AMPD3
0.882 0.040 11 10369034 intron variant G/A snv 0.21 5
rs7219021
TTLL6
0.925 0.040 17 48763179 intron variant T/G snv 0.26 4
rs781720548
CPNE1 ; RBM12
0.882 0.040 20 35652946 stop gained C/A snv 5
rs7872515
SPTLC1
0.925 0.040 9 92060258 intron variant G/A snv 0.25 4
rs802568
CNTNAP2
0.925 0.040 7 146262151 intron variant T/G snv 0.17 4
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 9
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs6994992
NRG1
0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs10275045
MAD1L1
0.882 0.160 7 1881190 intron variant C/T snv 0.35 5