Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10503929
NRG1
0.925 0.040 8 32756465 missense variant T/C snv 0.13 0.13 3
rs17512836
TCF4
0.925 0.040 18 55527730 intron variant T/C snv 2.2E-02 3
rs4949526 1.000 0.040 1 29959372 intergenic variant T/C snv 0.54 3
rs1341402
DAOA-AS1
1.000 0.040 13 105463160 intron variant T/C snv 0.16 2
rs1893490
MAPK4
1.000 0.040 18 50669431 non coding transcript exon variant T/C snv 0.48 2
rs2312147
VRK2
1.000 0.040 2 57995793 intron variant T/C snv 0.70 2
rs3761554
GRIA3
1.000 0.040 X 123183391 upstream gene variant T/C snv 0.21 2
rs502434
GRIA3
1.000 0.040 X 123403426 synonymous variant T/C snv 0.59 2
rs6932590 1.000 0.040 6 27281152 downstream gene variant T/C snv 0.26 2
rs7248363
PGPEP1
19 18357076 intron variant T/C snv 0.74 2
rs769404
GAD1
1.000 0.040 2 170822115 synonymous variant T/C snv 0.39 0.35 2
rs2076369
PICK1
0.925 0.040 22 38067645 non coding transcript exon variant T/A;G snv 3
rs35753505 0.827 0.080 8 31616625 intergenic variant T/A;C snv 6
rs3803300
ZBTB42
0.827 0.120 14 104803442 3 prime UTR variant T/A;C snv 6
rs1421292 0.925 0.040 13 105545886 intergenic variant T/A snv 0.39 3
rs12527359 6 89018502 intergenic variant T/A snv 0.23 2
rs713729
PICK1
1.000 0.040 22 38059462 intron variant T/A snv 0.20 2
rs4570625
TPH2
0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
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
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs2857766
MOG
0.882 0.120 6 29666226 missense variant G/C snv 0.22 0.19 4
rs1806864 9 87416754 regulatory region variant G/C snv 7.4E-02 2
rs7727102 5 4720472 intron variant G/C snv 0.32 2