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
rs2066702
ADH1B
0.882 0.080 4 99307860 missense variant G/A snv 1.5E-02 5.9E-02 7
rs10196867
CTNNA2
0.925 0.080 2 79751234 intron variant C/G;T snv 5
rs1039002
PDE10A
0.851 0.080 6 165741969 intron variant G/A;T snv 5
rs1079597
DRD2
0.827 0.080 11 113425564 intron variant C/T snv 0.18 5
rs139438618
SEMA3A
0.882 0.080 7 84008281 intron variant A/G snv 5.2E-02 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
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
rs6943555
AUTS2
0.882 0.080 7 70341037 intron variant T/A snv 0.34 5
rs10198241 0.925 0.080 2 226115660 intergenic variant T/C snv 0.58 4
rs1042363
AKAP12
0.882 0.080 6 151356693 3 prime UTR variant T/C snv 4
rs115357105 0.925 0.080 9 104376689 intergenic variant A/G snv 1.5E-02 4
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
rs12180309 0.925 0.080 6 91209048 intergenic variant C/T snv 1.9E-02 4
rs12544026
NCALD
0.925 0.080 8 101819970 intron variant G/A snv 0.85 4
rs17028615
LOC100507053 ; ADH4
1.000 0.080 4 99150767 intron variant A/C;G snv 4
rs1789882
ADH1B
1.000 0.080 4 99313896 synonymous variant A/G;T snv 0.82 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
rs2094081
RHBDL2
0.925 0.080 1 38927359 intron variant G/A;C snv 4