Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228612 0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14 12
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs230490 0.882 0.080 4 102466262 downstream gene variant G/A snv 0.34 3
rs4648110 0.925 0.080 4 102612664 intron variant T/A snv 0.22 3
rs997476 0.882 0.080 4 102620848 downstream gene variant G/T snv 4.3E-02 3
rs750521832 0.732 0.200 11 102718452 missense variant A/G snv 4.0E-06 14
rs7911488 0.882 0.080 10 103394332 5 prime UTR variant A/G snv 0.34 0.26 3
rs4135113
TDG
0.925 0.080 12 103982915 missense variant G/A;C;T snv 4.7E-02 5
rs2302615 0.807 0.120 2 10448012 intron variant C/T snv 0.31 7
rs1383147053
DLD
0.882 0.120 7 107901762 missense variant G/A snv 4
rs1805097 0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs773442580
EGF
0.851 0.080 4 109913367 missense variant T/C;G snv 4.0E-06 7
rs3802842 0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs777980327
APC
0.716 0.280 5 112837567 missense variant A/T snv 4.0E-06 7.0E-06 21
rs1380087059
APC
0.882 0.160 5 112837749 missense variant G/C snv 4.0E-06 3
rs587781394
APC
0.882 0.160 5 112837812 missense variant G/A;C snv 4.0E-06; 8.0E-06 3
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 42
rs459552
APC
0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 14
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 18
rs2770150 0.925 0.080 9 117700861 upstream gene variant A/G snv 0.22 4
rs10759932 0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18 15
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs11536898 0.882 0.080 9 117717932 3 prime UTR variant C/A snv 0.14 3