Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs900418273
ANKK1
0.807 0.120 11 113393764 missense variant A/G snv 8
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs1076560
DRD2
0.776 0.120 11 113412966 intron variant C/A snv 0.16 11
rs2734835
DRD2
1.000 0.080 11 113420621 intron variant T/G snv 0.43 1
rs1800498
DRD2
0.882 0.080 11 113420866 intron variant G/A snv 0.44 4
rs1116313
DRD2
1.000 0.080 11 113425385 intron variant A/G snv 0.45 1
rs1079597
DRD2
0.827 0.080 11 113425564 intron variant C/T snv 0.18 5
rs61902812 1.000 0.080 11 113503698 intergenic variant C/A snv 0.26 3
rs4936277 1.000 0.080 11 113561238 intergenic variant A/G snv 0.37 3
rs1176744
HTR3B
0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs2276305
HTR3B
1.000 0.080 11 113932382 synonymous variant G/A;C;T snv 7.7E-02; 2.8E-03; 5.2E-05 1
rs3782025
HTR3B
0.882 0.080 11 113936885 intron variant G/A snv 0.55 4
rs33940208
HTR3A
1.000 0.080 11 113975355 synonymous variant C/T snv 8.2E-02 7.0E-02 1
rs10160548
HTR3A
1.000 0.080 11 113985959 intron variant G/T snv 0.54 1
rs2134655
DRD3
0.925 0.080 3 114139354 intron variant C/A;T snv 2
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs727532
ABLIM1
1.000 0.080 10 114445017 intron variant A/G snv 0.17 1
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs141424017 1.000 0.080 7 115311376 intergenic variant -/CAA ins 3
rs363387
SLC18A2 ; LOC105378500
1.000 0.080 10 117244053 synonymous variant T/A;C;G snv 4.0E-06; 7.9E-02 1
rs13273672
GATA4
0.925 0.080 8 11754872 intron variant T/C snv 0.34 2
rs10892169
DSCAML1
1.000 0.080 11 117762339 intron variant A/G snv 0.68 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs7777391 1.000 0.080 7 117981823 intergenic variant A/G snv 0.60 1