Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs604300
MGLL
1.000 0.080 3 127724009 intron variant A/G snv 0.91 3
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs382140 7 108141755 intergenic variant A/G snv 0.74 1
rs4436578
DRD2
0.925 0.080 11 113436043 intron variant C/T snv 0.73 4
rs2180619
CNR1
1.000 0.040 6 88168233 upstream gene variant G/A snv 0.53 3
rs1333045
CDKN2B-AS1
0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 14
rs1040288
NR3C2
1.000 0.040 4 148126966 intron variant G/C snv 0.49 3
rs678849
OPRD1
0.882 0.120 1 28818676 intron variant C/T snv 0.44 5
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs2070762
TH
0.925 0.080 11 2165105 intron variant A/G snv 0.43 5
rs1875999
CRHBP
5 76969157 3 prime UTR variant T/C snv 0.38 1
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs230530
NFKB1
0.882 0.080 4 102532823 intron variant A/G snv 0.37 4
rs4648318
DRD2
1.000 0.080 11 113442667 intron variant T/C snv 0.33 2
rs2073837
DBH-AS1 ; DBH
9 133657806 intron variant G/A snv 0.31 1
rs9444584
CNR1
0.882 0.160 6 88152840 intron variant C/T snv 0.30 4
rs11503014
GABRA2
1.000 0.080 4 46388848 5 prime UTR variant C/G snv 0.27 2
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1611131
DBH-AS1 ; DBH
0.925 0.080 9 133657065 splice region variant A/G snv 0.28; 4.0E-06 0.25 3
rs1075650
IER5L
9 129176634 3 prime UTR variant T/C snv 0.25 1
rs7118900
ANKK1
11 113396099 missense variant G/A snv 0.25 0.25 1
rs963549
OPRK1
8 53229264 synonymous variant C/T snv 0.17 0.24 1
rs2023239
CNR1
0.724 0.160 6 88150763 intron variant T/C snv 0.21 20