Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs36053993
MUTYH
0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 31
rs150766139
NTHL1 ; TSC2
0.742 0.320 16 2046238 stop gained G/A snv 1.4E-03 1.4E-03 13
rs1761667
CD36
0.752 0.320 7 80615623 intron variant G/A snv 0.49 12
rs1057519945
POLE
0.776 0.200 12 132673703 missense variant C/A;T snv 12
rs483352909
POLE
0.752 0.160 12 132673664 missense variant G/A;C snv 1.6E-05 11
rs2266780
FMO3
0.827 0.280 1 171114102 missense variant A/G snv 0.15 0.14 9
rs1984112
CD36
0.807 0.280 7 80613604 intron variant A/G snv 0.33 8
rs1049673
CD36
0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 7
rs2266782
FMO3
0.851 0.200 1 171107825 missense variant G/A snv 0.37 0.41 7
rs63751310
MLH1
0.851 0.200 3 37048595 stop gained C/T snv 6
rs587780749
MUTYH
0.925 0.160 1 45332443 missense variant C/A;T snv 5.6E-05; 8.0E-06 5
rs397514632
POLD1
0.827 0.160 19 50406456 missense variant G/A snv 5
rs145236923
GALNT12
0.851 0.120 9 98831947 missense variant G/A snv 1.2E-03 1.3E-03 4
rs112422930
MUTYH
0.882 0.160 1 45332409 missense variant A/C snv 7.0E-06 4
rs121908380
MUTYH
0.882 0.160 1 45333449 stop gained G/A;T snv 1.4E-03; 1.2E-04 4
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
rs587783032
APC
1.000 0.040 5 112842342 missense variant G/A;T snv 4.0E-06 3
rs3211299
FBXO11 ; MSH6
0.882 0.200 2 47791097 missense variant G/T snv 9.4E-04 1.5E-03 3
rs200844166
MUTYH
0.882 0.160 1 45331240 missense variant G/T snv 2.4E-05 5.6E-05 3
rs34126013
MUTYH
0.925 0.160 1 45332458 missense variant G/A snv 6.8E-05 2.1E-05 3
rs730881834
MUTYH
0.882 0.120 1 45332181 missense variant G/C snv 3
rs743582
PML
1.000 0.040 15 74035865 missense variant G/A;C snv 2.8E-05; 0.12 3
rs142637152
APC
0.925 0.120 5 112767314 missense variant G/T snv 2