Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs314277 0.925 0.080 6 104959787 intron variant A/C;G;T snv 6
rs1535989 0.925 0.080 13 105370372 intergenic variant A/G;T snv 4
rs372032595
DLD
0.925 0.080 7 107904960 missense variant T/G snv 4.0E-06 3
rs189037
ATM ; NPAT
0.689 0.400 11 108223106 5 prime UTR variant G/A snv 0.49 22
rs1065411 0.925 0.080 1 109690516 missense variant G/A;C;T snv 0.36; 6.9E-06 2
rs1805097 0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs3802842 0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs201745983 0.752 0.200 12 111783219 missense variant G/A snv 6.8E-05 7.7E-05 14
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs12241008 0.716 0.160 10 112520943 intron variant T/C snv 0.13 16
rs10506868 0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 16
rs2295080 0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs79896135
APC
0.925 0.080 5 112707585 5 prime UTR variant C/A;G;T snv 2
rs11196067 0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs7086803 0.763 0.160 10 112738717 intron variant G/A snv 0.20 9
rs150973053
APC
0.851 0.200 5 112767356 missense variant A/G snv 3.5E-04 2.7E-04 4
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs2856838 0.851 0.200 2 112782395 intron variant G/A snv 0.37 4
rs530670052
APC
0.925 0.080 5 112801313 missense variant A/G snv 1.6E-05 1.4E-05 2
rs454886
APC
0.763 0.280 5 112810420 intron variant A/G snv 0.26 10
rs770649674
APC
0.807 0.120 5 112827177 missense variant A/G snv 4.0E-06 7.0E-06 6
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52