Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1137070
MAOA
0.763 0.160 X 43744144 synonymous variant T/C snv 0.62 9
rs1800973
LYZ
0.827 0.320 12 69350234 missense variant C/A snv 4.2E-02 4.3E-02 9
rs2066713
SLC6A4
0.807 0.200 17 30224647 intron variant G/A snv 0.34 9
rs35385902
ADH1C ; ADH1B
0.807 0.240 4 99347122 missense variant C/A;T snv 2.0E-05; 1.1E-03 9
rs3771829
TACR1
0.790 0.120 2 75137019 intron variant C/G snv 0.11 9
rs686
DRD1
0.807 0.080 5 175441697 3 prime UTR variant G/A;C;T snv 9
rs11568817
HTR1B ; LOC105377864
0.790 0.120 6 77463665 5 prime UTR variant A/C snv 0.37 8
rs130058
HTR1B ; LOC105377864
0.790 0.120 6 77463564 5 prime UTR variant T/A;G snv 8
rs1535255
CNR1
0.807 0.120 6 88151489 intron variant T/G snv 0.21 8
rs1806201
GRIN2B
0.776 0.200 12 13564574 synonymous variant G/A snv 0.32 0.24 8
rs279858
GABRA2
0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs769540300
OPRM1
0.851 0.200 6 154091047 missense variant G/A snv 1.2E-05 8
rs886205
ALDH2
0.827 0.360 12 111766623 intron variant A/G snv 0.35 8
rs900418273
ANKK1
0.807 0.120 11 113393764 missense variant A/G snv 8
rs1805502
GRIN2B
0.790 0.200 12 13561247 3 prime UTR variant A/G snv 0.25 7
rs2066702
ADH1B
0.882 0.080 4 99307860 missense variant G/A snv 1.5E-02 5.9E-02 7
rs4251417
SLC6A4
0.827 0.200 17 30224840 intron variant C/T snv 6.8E-02 7
rs10392
PPP1R16B
0.882 0.160 20 38922292 3 prime UTR variant G/A snv 0.17 6
rs1042114
OPRD1
0.807 0.120 1 28812463 missense variant G/C;T snv 0.91 6
rs10514299
TMEM161B-AS1
0.827 0.120 5 88367793 intron variant C/T snv 0.21 6
rs13212041
LOC105377864 ; HTR1B
0.851 0.200 6 77461407 downstream gene variant C/T snv 0.70 6
rs17037102
DKK2
0.807 0.240 4 106924637 missense variant C/A;T snv 0.15 6
rs2236418
GAD2
0.882 0.120 10 26216567 upstream gene variant A/G snv 0.36 6
rs29230
GABBR1
0.807 0.440 6 29608616 missense variant A/C;G snv 4.1E-06; 0.18 6
rs595961
AGO1
0.807 0.160 1 35902179 intron variant A/G snv 0.30 0.37 6