Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4906902
GABRB3
0.724 0.200 15 26774621 intron variant A/G snv 0.15 14
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13
rs3813867
LOC107984284 ; CYP2E1
0.732 0.240 10 133526101 intron variant G/A;C snv 13
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 12
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs11030104
BDNF ; BDNF-AS
0.790 0.240 11 27662970 intron variant A/G snv 0.16 12
rs2283265
DRD2
0.776 0.160 11 113414814 intron variant C/A snv 0.16 12
rs2710102
CNTNAP2
0.790 0.120 7 147877298 intron variant A/G;T snv 12
rs1076560
DRD2
0.776 0.120 11 113412966 intron variant C/A snv 0.16 11
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv 11
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins 11
rs2494732
AKT1
0.763 0.240 14 104772855 intron variant T/C snv 0.50 0.47 11
rs3116496
CD28
0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14 11
rs3213207
DTNBP1
0.776 0.120 6 15627871 intron variant T/C snv 8.7E-02 11
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 11
rs737865
TXNRD2 ; COMT
0.763 0.240 22 19942598 intron variant A/G snv 0.23 11
rs1417938
CRP
0.776 0.320 1 159714396 intron variant T/A;C snv 0.28 10
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 10
rs4251961
IL1RN
0.763 0.200 2 113116890 intron variant T/C snv 0.29 10
rs694539
NNMT
0.776 0.200 11 114262697 intron variant C/T snv 0.21 10
rs8042374
CHRNA3
0.807 0.200 15 78615690 intron variant A/G snv 0.29 10
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 9
rs17486278
CHRNA5
0.827 0.120 15 78575140 intron variant A/C snv 0.32 9
rs2066713
SLC6A4
0.807 0.200 17 30224647 intron variant G/A snv 0.34 9
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 9