Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10082479
CHAT
1.000 0.080 10 49621173 intron variant A/T snv 0.23 1
rs1042173
SLC6A4
0.763 0.320 17 30197993 3 prime UTR variant A/C snv 0.40 14
rs1044394
CHRNA4
1.000 0.080 20 63350733 synonymous variant A/G snv 0.92 0.81 1
rs1044396
CHRNA4
0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs1044397
CHRNA4
0.851 0.160 20 63349752 synonymous variant C/T snv 0.48 0.41 7
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs1079597
DRD2
0.827 0.080 11 113425564 intron variant C/T snv 0.18 5
rs10798059
PLA2G4A
0.925 0.080 1 186830478 intron variant G/A snv 0.40 2
rs10865246
NRXN1
1.000 0.080 2 50443116 intron variant C/A;T snv 1
rs1122530
NTRK2
1.000 0.080 9 84849437 intron variant A/G snv 0.22 1
rs1131339
STX17-AS1 ; NR4A3
0.925 0.080 9 99865020 3 prime UTR variant A/G snv 0.45 2
rs1137070
MAOA
0.763 0.160 X 43744144 synonymous variant T/C snv 0.62 9
rs11568817
HTR1B ; LOC105377864
0.790 0.120 6 77463665 5 prime UTR variant A/C snv 0.37 8
rs1162419578
APP
0.925 0.160 21 25975126 missense variant G/A snv 4.0E-06 2
rs11636753
CHRNB4
0.882 0.120 15 78636604 intron variant G/T snv 0.35 4
rs1176744
HTR3B
0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs1187272
NTRK2
1.000 0.080 9 84789171 intron variant G/A;C snv 1
rs12266458
CHAT
1.000 0.080 10 49639951 intron variant C/T snv 0.11 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs12466358
CHRND
1.000 0.080 2 232532815 intron variant T/G snv 0.22 1
rs12519
SHC3
1.000 0.080 9 89013167 3 prime UTR variant T/A;C snv 1
rs12718541
FIGNL1 ; DDC
0.925 0.080 7 50482446 intron variant A/G snv 0.55 2
rs12720071
CNR1
0.807 0.200 6 88141462 3 prime UTR variant T/C snv 0.11 7
rs130058
HTR1B ; LOC105377864
0.790 0.120 6 77463564 5 prime UTR variant T/A;G snv 8
rs1312171358
CNR1
1.000 0.080 6 88144597 synonymous variant C/T snv 8.0E-06 7.0E-06 1