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
rs4919687 0.742 0.160 10 102835491 non coding transcript exon variant G/A snv 0.25 6
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
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 5
rs1391441 0.763 0.240 4 105207603 intron variant G/A snv 0.70 1
rs1383147053
DLD
0.882 0.120 7 107901762 missense variant G/A snv 4
rs1364898025
ATM
0.925 0.080 11 108227656 missense variant G/A snv 3
rs1805097 0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 21
rs773442580
EGF
0.851 0.080 4 109913367 missense variant T/C;G snv 4.0E-06 7
rs3087967 0.776 0.080 11 111286111 3 prime UTR variant T/C snv 0.72 1
rs3802842 0.695 0.280 11 111300984 intron variant C/A snv 0.71 17
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 29
rs12241008 0.716 0.160 10 112520943 intron variant T/C snv 0.13 8
rs10506868 0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 8
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
rs137854575
APC
0.807 0.120 5 112838399 stop gained C/A;G;T snv 4.7E-04 1