Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 42
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs777980327
APC
0.716 0.280 5 112837567 missense variant A/T snv 4.0E-06 7.0E-06 21
rs1801166
APC
0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 17
rs121913224
APC
0.742 0.200 5 112839515 frameshift variant AAAGA/- delins 14
rs459552
APC
0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 14
rs11954856
APC
0.732 0.200 5 112751630 intron variant T/G snv 0.54 12
rs121913331
APC
0.851 0.120 5 112838934 stop gained C/A;T snv 8.0E-06 11
rs137854573
APC
0.807 0.120 5 112828889 stop gained C/T snv 10
rs454886
APC
0.763 0.280 5 112810420 intron variant A/G snv 0.26 10
rs786201856
APC
0.776 0.200 5 112815507 stop gained C/T snv 10
rs137854575
APC
0.807 0.120 5 112838399 stop gained C/A;G;T snv 4.7E-04 9
rs62619935
APC
0.807 0.120 5 112792446 stop gained C/G;T snv 4.0E-06 8
rs145945630
APC
0.827 0.120 5 112754960 stop gained C/T snv 2.4E-05 7
rs387906234
APC
0.827 0.120 5 112839979 frameshift variant AGAG/-;AG delins 7
rs397515734
APC
0.827 0.120 5 112792494 stop gained C/T snv 7
rs587781392
APC
0.827 0.120 5 112780895 stop gained C/G;T snv 7
rs587783031
APC
0.851 0.120 5 112840255 frameshift variant A/-;AA delins 7
rs863225311
APC
0.827 0.120 5 112819347 splice region variant A/C;G snv 7
rs121913333
APC
0.882 0.120 5 112838220 stop gained C/A;T snv 6
rs137854580
APC
0.827 0.120 5 112827194 stop gained C/G;T snv 2.8E-05 6
rs2229992
APC
0.827 0.200 5 112827157 stop gained T/C;G snv 0.58 0.47 6
rs770649674
APC
0.807 0.120 5 112827177 missense variant A/G snv 4.0E-06 7.0E-06 6
rs121913332
APC
0.925 0.120 5 112839942 stop gained C/G;T snv 4.0E-06 5
rs137854568
APC
0.882 0.120 5 112815564 stop gained C/T snv 5