Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042363
AKAP12
0.882 0.080 6 151356693 3 prime UTR variant T/C snv 4
rs1047383
PLCB1
20 8884359 3 prime UTR variant C/T snv 0.56 1
rs1076560
DRD2
0.776 0.120 11 113412966 intron variant C/A snv 0.16 11
rs10784339
AVPR1A
12 63144866 3 prime UTR variant G/A;C;T snv 1
rs1126671
ADH4 ; LOC100507053
0.851 0.120 4 99127263 missense variant T/C snv 0.76 0.75 5
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1255388379
OPRL1
20 64092838 missense variant G/A snv 2.1E-05 1
rs1262930152
LOC105378626 ; TINAGL1 ; LINC01226
1 31577384 missense variant G/A;T snv 8.0E-06 1
rs13438494
PCLO
1.000 0.040 7 82759398 intron variant T/G snv 0.61 6
rs1650420
GRIN2A
1.000 0.080 16 10174473 intron variant T/C snv 0.58 2
rs17228602
ACHE ; UFSP1
7 100890786 3 prime UTR variant C/T snv 1.5E-02 2
rs17228616
ACHE ; UFSP1
1.000 0.080 7 100890100 3 prime UTR variant G/T snv 9.8E-02 3
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
rs1800759
LOC100507053 ; ADH4
0.925 0.120 4 99144358 intron variant T/G snv 0.49 4
rs199953844
OPRM1
6 154039650 missense variant C/A;T snv 4.0E-06; 1.2E-04 2
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs279858
GABRA2
0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs3735451
CYP3A4
7 99758352 intron variant T/C snv 0.31 1
rs3743484
CYP1A2
15 74752059 intron variant G/C snv 3.7E-02 1
rs441
ALDH2
0.882 0.200 12 111791045 intron variant T/C snv 0.18 4
rs4646437
CYP3A4
0.827 0.200 7 99767460 intron variant G/A snv 0.30 8
rs4646440
CYP3A4
7 99763247 intron variant G/A snv 5.1E-02 2
rs4646778
MIR6761 ; ALDH2
12 111797979 intron variant C/A snv 0.18 1