Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1036199 0.925 0.160 5 157104725 missense variant C/A snv 0.87 0.83 3
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 16
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1059702 0.807 0.280 X 154018741 missense variant A/G snv 0.72 7
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3811047 0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60 10
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1800601 0.882 1 156815825 5 prime UTR variant G/A;T snv 0.67; 4.0E-06 4
rs1059703 0.851 0.280 X 154013378 missense variant G/A snv 0.67 6
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs30187 0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 14
rs1131017 0.925 0.160 12 56042145 5 prime UTR variant C/A;G;T snv 8.0E-06; 8.0E-06; 0.62; 1.1E-04 5
rs1126407 0.925 0.200 1 236537507 missense variant T/A snv 0.61 0.61 3
rs237025 0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs763361 0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 21
rs3827440 0.851 0.120 X 79171491 missense variant T/A;C snv 5.5E-06; 0.51 6
rs228648 0.776 0.360 1 7853370 missense variant G/A snv 0.51 0.52 13
rs1990760 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs2229080
DCC
0.742 0.320 18 52906232 missense variant C/A;G snv 0.45 16
rs945635 0.882 0.200 1 157700500 5 prime UTR variant C/A;G snv 5.6E-05; 0.45 4
rs12928404 0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 15
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs2076530 0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 17