Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1176744
HTR3B
0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs1042173
SLC6A4
0.763 0.320 17 30197993 3 prime UTR variant A/C snv 0.40 14
rs11568817
HTR1B ; LOC105377864
0.790 0.120 6 77463665 5 prime UTR variant A/C snv 0.37 8
rs7131056
DRD2
0.827 0.200 11 113459052 intron variant A/C snv 0.51 6
rs2734849
ANKK1
1.000 0.080 11 113399438 missense variant A/C;G snv 4.5E-06; 0.39 1
rs28399433
CYP2A6
0.827 0.200 19 40850474 intron variant A/C;G;T snv 0.10; 4.4E-06 7
rs910083
DNMT3B
1.000 0.080 20 32790884 intron variant A/C;G;T snv 2
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs2279343
CYP2B6
0.776 0.200 19 41009358 missense variant A/G snv 0.13 8
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
rs3733829
EGLN2 ; RAB4B-EGLN2
0.882 0.120 19 40804666 non coding transcript exon variant A/G snv 0.28 5
rs13273442 0.882 0.080 8 42688874 intergenic variant A/G snv 0.66 4
rs1451240 0.925 0.080 8 42691568 intergenic variant A/G snv 0.64 4
rs848353 1.000 0.080 7 108908603 upstream gene variant A/G snv 0.14 3
rs1131339
STX17-AS1 ; NR4A3
0.925 0.080 9 99865020 3 prime UTR variant A/G snv 0.45 2
rs12718541
FIGNL1 ; DDC
0.925 0.080 7 50482446 intron variant A/G snv 0.55 2
rs1044394
CHRNA4
1.000 0.080 20 63350733 synonymous variant A/G snv 0.92 0.81 1
rs1122530
NTRK2
1.000 0.080 9 84849437 intron variant A/G snv 0.22 1
rs1659400
NTRK2
1.000 0.080 9 84711079 intron variant A/G snv 0.60 1
rs2060762
FIGNL1 ; DDC
1.000 0.080 7 50461686 intron variant A/G snv 0.81 1
rs2297313
SHC3
1.000 0.080 9 89054447 intron variant A/G snv 0.41 1
rs4424567
FRMD4A
1.000 0.080 10 13759269 3 prime UTR variant A/G snv 0.25 1
rs507506
DLG4
1.000 0.080 17 7215003 intron variant A/G snv 0.55 1
rs774507706
OPRM1
1.000 0.080 6 154091093 missense variant A/G snv 4.0E-06 1