Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs686
DRD1
0.807 0.080 5 175441697 3 prime UTR variant G/A;C;T snv 9
rs279858
GABRA2
0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs10196867
CTNNA2
0.925 0.080 2 79751234 intron variant C/G;T snv 5
rs1079597
DRD2
0.827 0.080 11 113425564 intron variant C/T snv 0.18 5
rs147247472
AGBL4-IT1 ; AGBL4
0.925 0.080 1 49441901 intron variant G/A snv 7.3E-04 5
rs1799913
TPH1
0.851 0.080 11 18025708 splice region variant G/A;T snv 0.39 0.33 5
rs2133896
ANKS1B
0.925 0.080 12 99455122 intron variant G/T snv 7.6E-02 5
rs6943555
AUTS2
0.882 0.080 7 70341037 intron variant T/A snv 0.34 5
rs12364283
DRD2 ; LOC105369501
0.925 0.080 11 113476233 upstream gene variant A/G snv 5.8E-02 3
rs2236861
OPRD1
0.882 0.080 1 28813244 intron variant G/A snv 0.19 3
rs265981
DRD1
0.925 0.080 5 175443899 5 prime UTR variant A/G;T snv 3
rs10078866
DRD1
1.000 0.080 5 175445317 upstream gene variant A/G snv 5.2E-02 2
rs1022563
PDYN-AS1
0.925 0.080 20 1973693 intron variant C/G;T snv 2
rs11503014
GABRA2
1.000 0.080 4 46388848 5 prime UTR variant C/G snv 0.27 2
rs1389752
MPDZ
0.925 0.080 9 13235288 intron variant A/G;T snv 2
rs1530351
RGS9
0.925 0.080 17 65135491 intron variant G/A;C snv 2
rs1650420
GRIN2A
1.000 0.080 16 10174473 intron variant T/C snv 0.58 2
rs16917234
BDNF ; BDNF-AS
0.925 0.080 11 27676827 intron variant T/A;C snv 2
rs1816071
GABRB2
0.925 0.080 5 161332949 intron variant T/C snv 0.37 2
rs274622
GRM3
0.925 0.080 7 86643624 upstream gene variant C/T snv 0.67 2
rs3778150
OPRM1
0.925 0.080 6 154062523 intron variant T/C snv 0.17 2
rs3915568
NTSR1
0.925 0.080 20 62738120 intron variant T/C snv 0.19 2
rs4791230
RGS9
0.925 0.080 17 65136210 intron variant C/T snv 0.75 2
rs510769
OPRM1
1.000 0.080 6 154040884 intron variant C/T snv 0.25 2
rs62638690
OPRM1
0.925 0.080 6 154090110 missense variant G/T snv 5.6E-03 5.6E-03 2