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
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs2023239
CNR1
0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs2494732
AKT1
0.763 0.240 14 104772855 intron variant T/C snv 0.50 0.47 11
rs12720071
CNR1
0.807 0.200 6 88141462 3 prime UTR variant T/C snv 0.11 7
rs2295633
FAAH
0.827 0.120 1 46408711 intron variant A/G;T snv 7
rs2235749
PDYN-AS1 ; PDYN
0.790 0.200 20 1979293 3 prime UTR variant G/A snv 0.37 7
rs6454674
CNR1
0.851 0.120 6 88163211 intron variant T/G snv 0.32 5
rs9444584
CNR1
0.882 0.160 6 88152840 intron variant C/T snv 0.30 4
rs9450898
CNR1
0.925 0.160 6 88154344 intron variant C/T snv 0.21 3
rs1455858
LOC349160 ; CHRM2
0.925 0.080 7 136946956 intron variant T/C snv 0.69 3
rs1019238
ANKFN1
0.925 0.080 17 56201354 intron variant G/A;C snv 2
rs1431318
ANKFN1
0.925 0.080 17 56115162 intron variant A/G snv 0.64 2
rs806374
CNR1
0.925 0.080 6 88147601 intron variant T/C snv 0.37 2
rs56372821
EPHX2 ; GULOP
1.000 0.080 8 27578983 intron variant G/A snv 0.13 2
rs12491921
LOC101929485
0.925 0.080 3 106570103 intergenic variant T/C snv 0.44 2
rs57602752 1.000 0.080 10 118890460 intron variant A/C snv 9.0E-02 1
rs596359 1.000 0.080 6 153135918 upstream gene variant C/T snv 0.55 1
rs1339926621
CHRNA7
1.000 0.080 15 32153944 missense variant G/A snv 8.6E-06 1
rs12199654
MAPK14
1.000 0.080 6 36041718 intron variant A/G snv 4.2E-02 1