Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042114
OPRD1
0.807 0.120 1 28812463 missense variant G/C;T snv 0.91 6
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1789882
ADH1B
1.000 0.080 4 99313896 synonymous variant A/G;T snv 0.82 4
rs1042364
ADH4 ; LOC100507053
1.000 0.080 4 99124423 stop gained T/A;C snv 0.78 1
rs1126671
ADH4 ; LOC100507053
0.851 0.120 4 99127263 missense variant T/C snv 0.76 0.75 5
rs702859
KCNJ6
1.000 0.080 21 37625399 synonymous variant G/A snv 0.71 0.72 3
rs523349
SRD5A2
0.689 0.440 2 31580636 missense variant G/A;C;T snv 0.66; 4.9E-06 21
rs17689966
LINC02210-CRHR1 ; CRHR1 ; MAPT-AS1
1.000 0.080 17 45833089 intron variant G/A snv 0.63 0.56 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs1137070
MAOA
0.763 0.160 X 43744144 synonymous variant T/C snv 0.62 9
rs2501432
CNR2
0.716 0.480 1 23875430 missense variant T/C;G snv 0.62 16
rs2836016
KCNJ6
0.925 0.080 21 37840718 intron variant G/A snv 0.59 0.58 2
rs2234918
OPRD1
0.827 0.200 1 28863085 synonymous variant C/T snv 0.59 0.50 5
rs248793
SRD5A1 ; NSUN2
1.000 0.080 5 6633666 synonymous variant C/G snv 0.55 0.58 1
rs12529
AKR1C3
0.776 0.280 10 5094459 missense variant C/G snv 0.50 0.45 10
rs2567608
SSTR4
0.925 0.080 20 23036445 missense variant T/A;C snv 2.8E-05; 0.49 2
rs6715729
TACR1 ; LOC105374811
1.000 0.080 2 75198602 synonymous variant A/G snv 0.48 0.58 1
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs6356
TH
0.827 0.240 11 2169721 missense variant C/T snv 0.43 0.32 5
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs7301328
GRIN2B
0.882 0.120 12 13865843 synonymous variant G/C;T snv 0.41; 4.0E-06 3
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs279858
GABRA2
0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs1806191
GRIN2B
0.925 0.080 12 13563704 missense variant G/A;T snv 0.40; 4.0E-06 2