Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 48
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 35
rs121918487 0.716 0.440 10 121517378 missense variant C/A;G;T snv 24
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 21
rs79184941 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 18
rs121913403 0.683 0.240 3 41224622 missense variant C/A;G;T snv 14
rs121918491 0.716 0.440 10 121517371 synonymous variant C/T snv 4.0E-06 14
rs121913478 0.708 0.640 10 121515280 missense variant T/C snv 13
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 13
rs121434595 0.708 0.320 1 114716124 missense variant C/A;G;T snv 13
rs77543610 0.667 0.560 10 121520160 missense variant G/C snv 12
rs121913228 0.742 0.200 3 41224621 missense variant T/C;G snv 11
rs1057519044 0.752 0.440 10 121517390 missense variant C/T snv 11
rs1434545235 0.752 0.440 10 121565500 missense variant T/C snv 4.0E-06 11
rs1554927408 0.742 0.480 10 121515254 missense variant C/T snv 11
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 11
rs137854575
APC
0.807 0.120 5 112838399 stop gained C/A;G;T snv 4.7E-04 9
rs36053993 0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 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