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
rs1445081098
COMT ; MIR4761
0.724 0.480 22 19963746 missense variant G/C snv 4.0E-06 17
rs167771
DRD3
0.827 0.280 3 114157428 intron variant G/A;T snv 5