Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
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
rs1800532
TPH1
0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs165774
COMT
0.807 0.120 22 19965038 3 prime UTR variant G/A snv 0.27 11
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
rs686
DRD1
0.807 0.080 5 175441697 3 prime UTR variant G/A;C;T snv 9
rs2235749
PDYN-AS1 ; PDYN
0.790 0.200 20 1979293 3 prime UTR variant G/A snv 0.37 7
rs1042114
OPRD1
0.807 0.120 1 28812463 missense variant G/C;T snv 0.91 6
rs1799972
OPRM1
0.827 0.080 6 154039561 missense variant C/A;G;T snv 4.1E-06; 1.7E-02 6
rs1126671
ADH4 ; LOC100507053
0.851 0.120 4 99127263 missense variant T/C snv 0.76 0.75 5
rs2234918
OPRD1
0.827 0.200 1 28863085 synonymous variant C/T snv 0.59 0.50 5
rs678849
OPRD1
0.882 0.120 1 28818676 intron variant C/T snv 0.44 5
rs751416416
OPRK1
0.882 0.120 8 53250920 missense variant C/A;T snv 8.3E-06; 4.1E-06 5
rs1042363
AKAP12
0.882 0.080 6 151356693 3 prime UTR variant T/C snv 4
rs948854
GAL ; LOC107984343
0.882 0.200 11 68682735 upstream gene variant C/T snv 0.65 4
rs6985606
OPRK1
0.882 0.080 8 53248556 intron variant T/C snv 0.63 4
rs702764
OPRK1
0.925 0.120 8 53229597 synonymous variant T/C;G snv 0.17; 8.0E-06 4
rs997917
OPRK1
0.882 0.080 8 53239818 intron variant T/C snv 0.43 4
rs1997794
PDYN-AS1 ; PDYN
0.851 0.120 20 1994212 5 prime UTR variant T/C snv 0.50 4
rs910080
PDYN ; PDYN-AS1
0.851 0.120 20 1979580 3 prime UTR variant A/G snv 0.35 4
rs35349697
CREB1
0.882 0.080 2 207560294 synonymous variant G/A snv 8.0E-06 3