Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2186607 0.776 0.080 11 101785666 intron variant T/A snv 0.51 10
rs188096 1.000 0.080 13 103052694 missense variant A/C snv 0.85 0.89 1
rs41281678 1.000 0.080 13 103052700 synonymous variant G/A snv 1.9E-02 2.7E-02 1
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1391441 0.763 0.240 4 105207603 intron variant G/A snv 0.70 11
rs1078643 0.776 0.080 17 10803924 missense variant G/A;C snv 10
rs768623239 0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs1376251 0.882 0.160 12 10986253 missense variant C/T snv 0.40 0.28 3
rs8000189 0.776 0.080 13 110423534 intron variant C/T snv 0.61 10
rs10980628 0.776 0.080 9 110909123 intron variant T/C snv 0.16 10
rs3087967 0.776 0.080 11 111286111 3 prime UTR variant T/C snv 0.72 10
rs597808 0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
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
rs12246635 0.776 0.080 10 112528860 intron variant T/C snv 0.13 10
rs755229494
APC
0.776 0.080 5 112761654 intron variant A/G snv 9.6E-04 10
rs762117133
APC
1.000 0.080 5 112801324 missense variant C/A;T snv 2.4E-05 3
rs770649674
APC
0.807 0.120 5 112827177 missense variant A/G snv 4.0E-06 7.0E-06 6
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
rs1801166
APC
0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 17
rs11196170 0.776 0.080 10 112962862 intron variant G/A;C snv 10
rs13086367 0.776 0.080 3 113185041 downstream gene variant A/G snv 0.38 10
rs72942485
BOC
0.776 0.080 3 113280713 intron variant G/A snv 2.7E-02 4.5E-02 10
rs1427760 0.776 0.080 12 114662909 upstream gene variant T/C snv 0.49 10