Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913224
APC
0.742 0.200 5 112839515 frameshift variant AAAGA/- delins 13
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 10
rs755229494
APC
0.776 0.080 5 112761654 intron variant A/G snv 9.6E-04 10
rs137854575
APC
0.807 0.120 5 112838399 stop gained C/A;G;T snv 4.7E-04 9
rs137854573
APC
0.807 0.120 5 112828889 stop gained C/T snv 8
rs786201856
APC
0.776 0.200 5 112815507 stop gained C/T snv 8
rs145945630
APC
0.827 0.120 5 112754960 stop gained C/T snv 2.4E-05 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
rs62619935
APC
0.807 0.120 5 112792446 stop gained C/G;T snv 4.0E-06 7
rs863225311
APC
0.827 0.120 5 112819347 splice region variant A/C;G snv 7
rs876660765
APC
0.851 0.120 5 112815594 splice donor variant G/A snv 6
rs121913331
APC
0.851 0.120 5 112838934 stop gained C/A;T snv 8.0E-06 5
rs1554085355
APC
0.851 0.120 5 112839461 stop gained T/A snv 5
rs137854580
APC
0.827 0.120 5 112827194 stop gained C/G;T snv 2.8E-05 4
rs121913327
APC
0.925 0.120 5 112839606 stop gained C/G;T snv 3
rs1400295986
APC
0.925 0.080 5 112838233 missense variant T/C snv 2
rs1801166
APC
0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 1
rs459552
APC
0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 1
rs779998847
APC
1.000 0.080 5 112838262 missense variant G/A snv 8.0E-06 1