Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519891
ERBB3
0.851 0.160 12 56088557 missense variant G/A;T snv 4.0E-06 6
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
rs863225311
APC
0.827 0.120 5 112819347 splice region variant A/C;G snv 7
rs62619935
APC
0.807 0.120 5 112792446 stop gained C/G;T snv 4.0E-06 8
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 10
rs786201856
APC
0.776 0.200 5 112815507 stop gained C/T snv 10
rs1057519044
FGFR2
0.752 0.440 10 121517390 missense variant C/T snv 11
rs1434545235
FGFR2
0.752 0.440 10 121565500 missense variant T/C snv 4.0E-06 11
rs1554927408
FGFR2
0.742 0.480 10 121515254 missense variant C/T snv 12
rs121913228
CTNNB1
0.742 0.200 3 41224621 missense variant T/C;G snv 14
rs121918491
FGFR2
0.716 0.440 10 121517371 synonymous variant C/T snv 4.0E-06 15
rs121913478
FGFR2
0.708 0.640 10 121515280 missense variant T/C snv 17
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 19
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs121913403
CTNNB1
0.683 0.240 3 41224622 missense variant C/A;G;T snv 23
rs121918487
FGFR2
0.716 0.440 10 121517378 missense variant C/A;G;T snv 25
rs77543610
FGFR2
0.667 0.560 10 121520160 missense variant G/C snv 28
rs36053993
MUTYH
0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 31
rs34612342
MUTYH
0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 32
rs121913281
PIK3CA
0.623 0.520 3 179234296 missense variant C/T snv 37
rs79184941
FGFR2
0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 41
rs895819
MIR23A ; LOC284454 ; MIR27A ; MIR24-2
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46