Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs17576
MMP9
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs4633
COMT ; MIR4761
0.695 0.400 22 19962712 synonymous variant C/T snv 0.46 0.45 25
rs8040868
CHRNA3
0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 17
rs143383
GDF5
0.724 0.320 20 35438203 5 prime UTR variant G/A snv 0.47 17
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs11030104
BDNF ; BDNF-AS
0.790 0.240 11 27662970 intron variant A/G snv 0.16 12
rs886205
ALDH2
0.827 0.360 12 111766623 intron variant A/G snv 0.35 8
rs1676486
COL11A1
0.851 0.120 1 102888582 missense variant A/G;T snv 0.80; 4.0E-06 7
rs10490571
IL1R1
0.827 0.320 2 102100877 intron variant C/T snv 0.29 5
rs11030096
BDNF-AS
0.925 0.160 11 27643996 intron variant T/A;C snv 3
rs2615977
COL11A1
0.925 0.080 1 102986836 intron variant A/C snv 0.27 3
rs11066028
ALDH2
1.000 0.080 12 111807366 intron variant A/C snv 0.45 2
rs7296651
ALDH2
0.925 0.160 12 111809150 intron variant C/A;G snv 2
rs7481311
BDNF-AS
0.925 0.160 11 27561582 intron variant T/C snv 0.75 2
rs956730
IL1R1
0.925 0.120 2 102141656 intron variant G/A snv 0.42 2
rs375081888
NOS1
0.925 0.120 12 117331048 missense variant C/T snv 2.4E-05 7.0E-06 2
rs9406328
THBS2 ; LOC101929523
1.000 0.080 6 169234915 splice region variant G/A snv 0.37 0.31 2
rs11030064
BDNF-AS
1.000 0.080 11 27596469 intron variant C/T snv 0.41 1
rs62413038
EYS ; LOC107986608
1.000 0.080 6 63952008 intron variant T/A;G snv 0.49 1
rs9450607
EYS ; LOC107986608
1.000 0.080 6 64025138 intron variant A/G snv 0.32 1
rs6651255
GSDMC
1.000 0.080 8 129711546 intron variant T/A;C snv 1