Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8040868
CHRNA3
0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 17
rs578776
CHRNA3
0.742 0.240 15 78596058 3 prime UTR variant G/A snv 0.39 13
rs806368
CNR1
0.752 0.280 6 88140381 3 prime UTR variant T/C snv 0.19 14
rs1042173
SLC6A4
0.763 0.320 17 30197993 3 prime UTR variant A/C snv 0.40 14
rs31489
CLPTM1L
0.763 0.320 5 1342599 intron variant C/A snv 0.41 10
rs1137070
MAOA
0.763 0.160 X 43744144 synonymous variant T/C snv 0.62 9
rs2279343
CYP2B6
0.776 0.200 19 41009358 missense variant A/G snv 0.13 8
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
rs27072
SLC6A3
0.807 0.120 5 1394407 3 prime UTR variant C/A;T snv 11
rs686
DRD1
0.807 0.080 5 175441697 3 prime UTR variant G/A;C;T snv 9
rs4767364
NAA25
0.807 0.160 12 112083644 intron variant G/A snv 0.45 8
rs12720071
CNR1
0.807 0.200 6 88141462 3 prime UTR variant T/C snv 0.11 7
rs1801272
CYP2A6
0.807 0.240 19 40848628 missense variant A/T snv 2.0E-02 1.8E-02 6
rs1800955
DRD4
0.827 0.160 11 636784 upstream gene variant T/C;G snv 8
rs1573496
ADH7
0.827 0.160 4 99428512 missense variant C/G snv 8.5E-02; 4.9E-04 7.8E-02 7
rs28399433
CYP2A6
0.827 0.200 19 40850474 intron variant A/C;G;T snv 0.10; 4.4E-06 7
rs4105144 0.827 0.160 19 40852719 intron variant T/C snv 7
rs4532
DRD1
0.827 0.160 5 175443147 5 prime UTR variant C/T snv 0.68 0.72 7
rs2030324
BDNF
0.827 0.120 11 27705368 intron variant A/G snv 0.49 6
rs588765
CHRNA5
0.827 0.200 15 78573083 intron variant T/A;C snv 6
rs7131056
DRD2
0.827 0.200 11 113459052 intron variant A/C snv 0.51 6
rs1079597
DRD2
0.827 0.080 11 113425564 intron variant C/T snv 0.18 5
rs1948
CHRNB4
0.827 0.160 15 78625057 synonymous variant A/G;T snv 0.69 5
rs324650
LOC349160 ; CHRM2
0.827 0.080 7 137008914 intron variant T/A snv 0.55 5