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
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs4633
COMT ; MIR4761
0.695 0.400 22 19962712 synonymous variant C/T snv 0.46 0.45 25
rs7439366
UGT2B7
0.752 0.320 4 69098620 missense variant T/C snv 0.56 0.57 16
rs769540300
OPRM1
0.851 0.200 6 154091047 missense variant G/A snv 1.2E-05 8
rs765502022
UGT2B7
0.827 0.240 4 69112695 missense variant T/C snv 1.6E-05 8
rs8007267 0.882 0.200 14 54912273 intergenic variant C/T snv 0.31 6
rs1718125
LOC105370032 ; P2RX7
0.851 0.200 12 121155216 intron variant C/T snv 0.15 0.19 6
rs373611092
MIR4761 ; COMT
0.925 0.160 22 19962794 missense variant A/G snv 8.4E-05 4.9E-05 5
rs2234918
OPRD1
0.827 0.200 1 28863085 synonymous variant C/T snv 0.59 0.50 5
rs3783641
GCH1
0.882 0.120 14 54893421 intron variant T/A;C snv 0.25 4
rs2835859
KCNJ6
0.925 0.200 21 37645860 intron variant T/C snv 0.16 3
rs533123
OPRD1
0.882 0.160 1 28814643 intron variant G/A;C snv 3
rs13093031 1.000 0.120 3 88809891 intergenic variant A/G snv 0.17 2
rs6961071 1.000 0.120 7 156182007 downstream gene variant A/G;T snv 0.47 2
rs1288779666
NDUFA6-DT ; CYP2D6 ; LOC112268294
1.000 0.120 22 42128944 missense variant C/G snv 2
rs76060075
NDUFA6-DT ; CYP2D6 ; LOC112268294
1.000 0.120 22 42129185 missense variant C/G snv 2
rs749415280
UGT2B7
1.000 0.120 4 69096638 missense variant A/G snv 2
rs10483636 1.000 0.120 14 54334127 intergenic variant A/G snv 7.2E-02 1
rs1473203326
CYP2D6 ; NDUFA6-DT ; LOC112268294
1.000 0.120 22 42128215 missense variant G/A snv 1
rs1187761291
OPRM1
1.000 0.120 6 154039569 missense variant A/G snv 4.1E-06 1
rs200811844
OPRM1
1.000 0.120 6 154091110 missense variant T/C snv 1.8E-04 7.8E-04 1