Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs629849 0.827 0.160 6 160073377 missense variant A/C;G;T snv 0.90 0.91 9
rs1950902 0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 11
rs9869263 0.925 0.080 3 190312891 synonymous variant A/C;G;T snv 8.0E-06; 0.83; 4.0E-06 3
rs459552
APC
0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 14
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs4562 0.925 0.080 17 7260420 missense variant A/G snv 0.65 0.70 3
rs2228226 0.851 0.160 12 57472038 missense variant G/C snv 0.60 0.68 6
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs352139 0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs9344 0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 34
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs3804099 0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs9904341 0.695 0.280 17 78214286 5 prime UTR variant G/A;C;T snv 0.38; 4.8E-06 20
rs1799929 0.776 0.240 8 18400484 synonymous variant C/T snv 0.36 0.36 11
rs1805097 0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs975263 0.827 0.120 7 20158817 stop gained G/A;T snv 0.34 7
rs7911488 0.882 0.080 10 103394332 5 prime UTR variant A/G snv 0.34 0.26 3