Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs105633 0.882 0.040 5 141945684 synonymous variant T/C;G snv 0.98; 4.0E-06 3
rs1202874 1.000 0.040 X 151179756 intron variant C/G;T snv 7.0E-06; 0.83 1
rs140504 0.882 0.040 22 23285182 missense variant A/G snv 0.81 0.86 3
rs1062613 0.807 0.080 11 113975284 5 prime UTR variant T/C snv 0.79 0.71 7
rs4523096 1.000 0.040 6 152472277 intron variant C/A snv 0.76 0.79 1
rs6971 0.742 0.200 22 43162920 missense variant A/G snv 0.76 0.75 11
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1618355 0.925 0.040 21 44406579 intron variant C/A;G snv 0.73; 1.7E-05 2
rs1051375 1.000 0.040 12 2679713 synonymous variant G/A snv 0.68 0.57 1
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs12476147 0.851 0.040 2 184936178 missense variant A/T snv 0.66 0.59 4
rs919390 1.000 0.040 19 41966898 missense variant G/C;T snv 0.65; 6.5E-06 0.69 1
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs2070615 1.000 0.040 12 48824388 intron variant A/C;G snv 4.7E-06; 0.58 1
rs4290270 0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 17
rs734312 0.790 0.240 4 6301627 missense variant G/A snv 0.55 0.42 10
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs169068 0.742 0.280 16 1079872 missense variant C/T snv 0.54 0.50 12
rs2279574 0.827 0.120 12 89351700 missense variant C/A;T snv 0.52 8
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2710323 0.851 0.080 3 52781889 intron variant T/C snv 0.49 0.54 7
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1108580
DBH
0.790 0.240 9 133639992 splice region variant A/G snv 0.45 0.54 9
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs2302417 1.000 0.040 3 52780240 non coding transcript exon variant T/A snv 0.44; 3.1E-03; 1.5E-04; 1.0E-05 0.42 1