Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs370795352 0.742 0.360 10 87933163 missense variant T/A;C snv 4.0E-06 13
rs72653744 0.807 0.320 16 16163009 stop gained G/A snv 1.7E-04 1.2E-04 12
rs80358920 0.732 0.400 13 32346841 stop gained C/G;T snv 12
rs80359200 0.752 0.320 13 32394726 stop gained C/A;G snv 8.0E-06 12
rs1224040268 0.742 0.360 10 87931091 splice donor variant T/A;C snv 7.0E-06 12
rs28897756 0.752 0.440 13 32379913 splice region variant G/A;C;T snv 4.0E-06 11
rs80358435 0.752 0.440 13 32319154 stop gained G/C;T snv 4.0E-06; 4.0E-06 11
rs80358721 0.724 0.320 13 32339320 stop gained C/A;G;R snv 4.2E-06 11
rs80358814 0.742 0.440 13 32340212 stop gained G/T snv 8.0E-06 11
rs80358972 0.742 0.480 13 32356472 stop gained C/A;T snv 8.0E-06; 3.2E-05 11
rs80359212 0.763 0.320 13 32394814 stop gained C/T snv 1.2E-05 4.2E-05 11
rs7014346 0.732 0.240 8 127412547 intron variant A/G snv 0.63 11
rs121913396 0.732 0.200 3 41224607 missense variant A/C;G;T snv 11
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 11
rs1057520005 0.742 0.360 17 7673800 missense variant C/A;G snv 11
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 10
rs28897672 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 10
rs397507404 0.763 0.320 13 32370955 splice acceptor variant G/A;T snv 10
rs41293511 0.763 0.320 13 32363369 missense variant G/A;C snv 7.0E-06 10
rs80358391 0.763 0.320 13 32319109 stop gained G/A;T snv 4.0E-06 10
rs80358427 0.776 0.280 13 32332877 stop gained A/T snv 4.0E-06 10
rs80358557 0.763 0.320 13 32337464 stop gained C/A;T snv 4.0E-06; 4.0E-06 10
rs80358893 0.763 0.320 13 32341011 stop gained C/G snv 10
rs80359014 0.763 0.320 13 32362596 missense variant A/G;T snv 10
rs80359031 0.763 0.320 13 32363190 missense variant A/T snv 10