Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1136905 0.882 0.120 6 32518660 missense variant T/A;C snv 4.2E-03 3
rs11683487
NMI
0.882 0.120 2 151286035 intron variant G/T snv 0.36 3
rs121964872 0.882 0.120 16 68833362 missense variant A/G snv 4.4E-05 1.1E-04 3
rs13063604 0.882 0.120 3 128085887 intron variant G/A snv 0.23 3
rs147961867 0.882 0.120 16 30121998 missense variant T/C snv 5.6E-05 2.8E-05 3
rs1516982 0.882 0.120 8 128521400 intron variant A/G snv 0.16 3
rs1649942 0.925 0.120 10 82191935 intron variant G/A;C snv 3
rs1805129 0.882 0.120 22 28734470 synonymous variant T/C snv 3.6E-02 4.0E-02 3
rs186724 0.882 0.120 1 110018293 intron variant C/G;T snv 3
rs2191249 0.882 0.120 17 61758503 intron variant T/G snv 0.79 3
rs2228026 0.882 0.120 14 20395890 synonymous variant A/G snv 4.7E-02 3.8E-02 3
rs2252673 0.882 0.120 19 7150407 intron variant C/G snv 0.75 3
rs2287497 0.882 0.120 17 7689462 intron variant G/A snv 0.25 3
rs266851 0.882 0.120 19 50833083 intron variant C/T snv 0.20 3
rs34529039 0.882 0.120 19 33301725 synonymous variant C/A snv 0.19 0.16 3
rs35068177 0.882 0.120 7 87550213 synonymous variant T/C snv 2.2E-04 3.1E-04 3
rs351771
APC
0.882 0.120 5 112828864 synonymous variant G/A snv 0.65 0.59 3
rs3976507 0.882 0.120 3 179239995 3 prime UTR variant C/T snv 0.19 0.24 3
rs4320932 0.882 0.120 11 2150371 intron variant T/C snv 0.19 3
rs4648551 0.882 0.120 1 3716166 intron variant G/A snv 0.32 3
rs4954956 0.882 0.120 2 138787007 regulatory region variant C/T snv 0.25 3
rs55854959 0.882 0.120 13 32330979 missense variant G/A snv 2.4E-05 1.4E-04 3
rs56318008 0.925 0.120 1 22143914 5 prime UTR variant C/T snv 0.13 3
rs567534295 0.882 0.120 17 43048090 intron variant C/T snv 2.8E-05 3
rs587780191 0.882 0.120 22 28699931 missense variant T/C;G snv 4.0E-06; 1.6E-05 3