Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913478
FGFR2
0.708 0.640 10 121515280 missense variant T/C snv 17
rs121913228
CTNNB1
0.742 0.200 3 41224621 missense variant T/C;G snv 14
rs1554927408
FGFR2
0.742 0.480 10 121515254 missense variant C/T snv 12
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
rs1057519891
ERBB3
0.851 0.160 12 56088557 missense variant G/A;T snv 4.0E-06 6
rs121918505
FGFR2
0.851 0.080 10 121520119 missense variant A/G snv 5
rs140342925
MUTYH
0.882 0.120 1 45332445 missense variant C/T snv 8.4E-05 8.4E-05 5
rs28933369
MIR4728 ; ERBB2
0.925 0.080 17 39724744 missense variant G/A snv 5
rs1057519803
ERBB3
0.925 0.080 12 56088138 missense variant G/A snv 4
rs1452231640
POLB
1.000 0.080 8 42339015 missense variant T/C snv 4.0E-06 4
rs1057519836
CTNNB1
3 41224630 missense variant A/C;G;T snv 2
rs121908382
MUTYH
1.000 0.080 1 45331530 missense variant G/A snv 2
rs121908383
MUTYH
1.000 0.080 1 45331502 missense variant T/C snv 2
rs121909776
CASP10
1.000 0.080 2 201187798 missense variant T/C snv 1.2E-04 2.8E-05 2
rs121912469
IRF1
1.000 0.080 5 132489457 missense variant T/A snv 2
rs1440200916
PDGFRA
4 54258803 missense variant G/C;T snv 2
rs149633775
TP53
1.000 0.120 17 7673773 missense variant G/A;C;T snv 7.2E-05; 4.0E-06 2
rs28933379
APC
1.000 0.080 5 112838953 missense variant G/A snv 2
rs121909144
KLF6
10 3781852 missense variant G/A;T snv 1
rs1342376116
ARID1A
1 26696438 missense variant G/T snv 1
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
rs121918491
FGFR2
0.716 0.440 10 121517371 synonymous variant C/T snv 4.0E-06 15
rs876660765
APC
0.851 0.120 5 112815594 splice donor variant G/A snv 6
rs1553125914
MUTYH
1.000 0.120 1 45331512 frameshift variant -/TC delins 2