Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs2023239
CNR1
0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs31489
CLPTM1L
0.763 0.320 5 1342599 intron variant C/A snv 0.41 10
rs4767364
NAA25
0.807 0.160 12 112083644 intron variant G/A snv 0.45 8
rs6495308
CHRNA3
0.851 0.160 15 78615314 intron variant T/C snv 0.29 8
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
rs1317286
CHRNA3
0.925 0.120 15 78603787 intron variant A/G snv 0.30 6
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
rs324650
LOC349160 ; CHRM2
0.827 0.080 7 137008914 intron variant T/A snv 0.55 5
rs9332377
ARVCF ; COMT
0.882 0.120 22 19968169 intron variant C/A;T snv 5
rs11636753
CHRNB4
0.882 0.120 15 78636604 intron variant G/T snv 0.35 4
rs2835859
KCNJ6
0.925 0.200 21 37645860 intron variant T/C snv 0.16 3
rs68081839
GRIA4
0.882 0.080 11 105762027 intron variant TT/-;T;TTT;TTTT;TTTTT;TTTTTTTTTTTT delins 3
rs10798059
PLA2G4A
0.925 0.080 1 186830478 intron variant G/A snv 0.40 2
rs12718541
FIGNL1 ; DDC
0.925 0.080 7 50482446 intron variant A/G snv 0.55 2
rs1909884
CHRNA7
0.925 0.120 15 32147097 intron variant G/A snv 0.41 2
rs2337980
CHRNA7
0.925 0.120 15 32151995 intron variant C/T snv 0.45 2
rs3793790
CHAT
0.925 0.120 10 49632690 intron variant G/A;C snv 2