Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800532
TPH1
0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs1076560
DRD2
0.776 0.120 11 113412966 intron variant C/A snv 0.16 11
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins 11
rs678849
OPRD1
0.882 0.120 1 28818676 intron variant C/T snv 0.44 5
rs6985606
OPRK1
0.882 0.080 8 53248556 intron variant T/C snv 0.63 4
rs997917
OPRK1
0.882 0.080 8 53239818 intron variant T/C snv 0.43 4
rs2236861
OPRD1
0.882 0.080 1 28813244 intron variant G/A snv 0.19 3
rs1022563
PDYN-AS1
0.925 0.080 20 1973693 intron variant C/G;T snv 2
rs12104412
ZNF565
1.000 0.080 19 36240156 intron variant A/G;T snv 4.2E-02 2
rs6473797
OPRK1
0.925 0.080 8 53240422 intron variant T/C snv 0.39 2
rs10854142
ZNF699
1.000 0.080 19 9302780 intron variant A/G snv 0.59 1
rs12460279
ZNF699
1.000 0.080 19 9300678 intron variant A/G snv 0.45 1
rs199774
LOC284788
1.000 0.080 20 22404679 intron variant G/A snv 0.32 1
rs2738888
DISC1 ; TSNAX-DISC1
1.000 0.080 1 231791308 intron variant C/G;T snv 1
rs6090041
OPRL1 ; RGS19
1.000 0.080 20 64081323 intron variant G/A snv 0.64 1
rs6419156
EMCN
1.000 0.080 4 100827029 intron variant G/A snv 0.26 1
rs7252865
ZNF699
1.000 0.080 19 9301859 intron variant C/A;T snv 1
rs821722
TSNAX-DISC1 ; DISC1
1.000 0.080 1 231900284 intron variant G/A snv 0.43 1
rs12442183
LOC105370980
1.000 0.080 15 93204756 intergenic variant C/T snv 0.38 2
rs73568641 1.000 0.080 6 153704004 intergenic variant T/C snv 0.14 2
rs9360217 1.000 0.080 6 66628700 intergenic variant T/G snv 0.21 2
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
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