Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs279871
GABRA2
0.882 0.080 4 46303716 intron variant T/C snv 0.38 5
rs324650
LOC349160 ; CHRM2
0.827 0.080 7 137008914 intron variant T/A snv 0.55 5
rs3764435
ALDH1A1
0.827 0.120 9 72901960 intron variant A/C;T snv 5
rs6943555
AUTS2
0.882 0.080 7 70341037 intron variant T/A snv 0.34 5
rs11681792
NRXN1
1.000 0.080 2 49957256 intron variant C/T snv 0.12 4
rs11825659
IGSF9B
0.925 0.080 11 133925624 intron variant A/G snv 0.12 4
rs12544026
NCALD
0.925 0.080 8 101819970 intron variant G/A snv 0.85 4
rs1614972
ADH1B ; ADH1C
0.925 0.160 4 99336998 intron variant C/T snv 0.38 4
rs17028615
LOC100507053 ; ADH4
1.000 0.080 4 99150767 intron variant A/C;G snv 4
rs1789891
ADH1B
1.000 0.080 4 99329262 intron variant C/A snv 0.13 4
rs1800498
DRD2
0.882 0.080 11 113420866 intron variant G/A snv 0.44 4
rs1800759
LOC100507053 ; ADH4
0.925 0.120 4 99144358 intron variant T/G snv 0.49 4
rs1824024
CHRM2 ; LOC349160
0.851 0.160 7 136958947 intron variant C/A snv 0.65 4
rs2094081
RHBDL2
0.925 0.080 1 38927359 intron variant G/A;C snv 4
rs2239803
HLA-DRA
0.882 0.240 6 32444056 intron variant C/A;T snv 0.50 4
rs2273816
KPNA3
0.851 0.080 13 49719920 intron variant G/A;C snv 4
rs279826
GABRA2
1.000 0.080 4 46332192 intron variant A/G snv 0.46 4
rs34997829
LHPP
1.000 0.080 10 124546821 intron variant G/C snv 0.24 4
rs3782025
HTR3B
0.882 0.080 11 113936885 intron variant G/A snv 0.55 4
rs58598658
KLF12
0.925 0.080 13 73887725 intron variant -/A;AA delins 4
rs7254880
ZNF699
0.882 0.160 19 9298599 intron variant C/G snv 0.16 4
rs72737330
ESRRG
0.925 0.080 1 216600151 intron variant T/C snv 0.15 4
rs79246196
STAG3
0.925 0.080 7 100185286 intron variant C/T snv 1.8E-02 4
rs1000579
STX18-AS1
1.000 0.080 4 4717767 intron variant A/G snv 0.44 3
rs10211296
CSRNP3
1.000 0.080 2 165633833 intron variant A/G snv 0.34 3