Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs1057519945 0.776 0.200 12 132673703 missense variant C/A;T snv 12
rs1761667 0.752 0.320 7 80615623 intron variant G/A snv 0.49 12
rs1984112 0.807 0.280 7 80613604 intron variant A/G snv 0.33 8
rs1049673 0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 7
rs63751310 0.851 0.200 3 37048595 stop gained C/T snv 6
rs397514632 0.827 0.160 19 50406456 missense variant G/A snv 5
rs112422930 0.882 0.160 1 45332409 missense variant A/C snv 7.0E-06 4
rs730881834 0.882 0.120 1 45332181 missense variant G/C snv 3
rs142637152
APC
0.925 0.120 5 112767314 missense variant G/T snv 2
rs555986369 1.000 0.040 2 47463080 missense variant G/A snv 4.0E-06 1
rs750902138
APC
1.000 0.040 5 112827226 synonymous variant T/G snv 4.0E-06 1
rs587783032
APC
1.000 0.040 5 112842342 missense variant G/A;T snv 4.0E-06 3
rs768299607 1.000 0.040 2 47799253 missense variant G/A;C snv 8.0E-06 1
rs587780749 0.925 0.160 1 45332443 missense variant C/A;T snv 5.6E-05; 8.0E-06 5
rs483352909 0.752 0.160 12 132673664 missense variant G/A;C snv 1.6E-05 11
rs200844166 0.882 0.160 1 45331240 missense variant G/T snv 2.4E-05 5.6E-05 3
rs743582
PML
1.000 0.040 15 74035865 missense variant G/A;C snv 2.8E-05; 0.12 3
rs202199891
APC
0.925 0.080 5 112827969 missense variant T/C snv 3.2E-05 2.1E-05 3
rs559313229
APC
1.000 0.040 5 112837797 missense variant G/C snv 3.2E-05 3
rs34126013 0.925 0.160 1 45332458 missense variant G/A snv 6.8E-05 2.1E-05 3
rs121908380 0.882 0.160 1 45333449 stop gained G/A;T snv 1.4E-03; 1.2E-04 4
rs146347092 1.000 0.040 16 2040004 stop gained G/A snv 1.8E-04 2.5E-04 1
rs9282599
APC
1.000 0.040 5 112827187 synonymous variant A/T snv 4.7E-04 1.9E-04 1
rs3211299 0.882 0.200 2 47791097 missense variant G/T snv 9.4E-04 1.5E-03 3