Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs864309486
GMNN
0.763 0.320 6 24777262 stop gained A/T snv 21
rs864309487
GMNN
0.763 0.280 6 24777279 frameshift variant TCAA/- delins 20
rs1445081098
COMT ; MIR4761
0.724 0.480 22 19963746 missense variant G/C snv 4.0E-06 17
rs864309488
GMNN
0.776 0.440 6 24777296 missense variant A/G snv 14
rs167771
DRD3
0.827 0.280 3 114157428 intron variant G/A;T snv 5
rs143141689
ORC1
0.882 0.280 1 52397773 missense variant C/T snv 9.5E-05 1.6E-04 3
rs374279734
ASPH
0.925 0.280 8 61653585 missense variant T/C snv 8.0E-06 4.2E-05 2
rs387906917
CDT1
0.925 0.200 16 88807390 missense variant G/A snv 5.6E-05 5.6E-05 2
rs1437544261
DONSON
0.925 0.280 21 33581303 missense variant T/C snv 7.0E-06 2
rs774052186
DONSON
0.925 0.280 21 33584744 missense variant G/A snv 2