Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913277
PIK3CA
0.925 0.280 3 179234302 missense variant G/A;C snv 4
rs121913289
PTEN
1.000 0.080 10 87958013 frameshift variant A/- delins 4
rs121913332
APC
0.925 0.120 5 112839942 stop gained C/G;T snv 4.0E-06 5
rs1057519862
ERBB2
0.851 0.160 17 39723405 missense variant G/A snv 5
rs1057519728
MAP2K1
0.851 0.120 15 66435103 missense variant T/A;C;G snv 5
rs1057519841
PIK3R1
0.925 0.120 5 68295269 missense variant A/G snv 5
rs1057519944
POLE
0.882 0.160 12 132676599 missense variant G/A snv 5
rs1057519952
RHOA
0.882 0.160 3 49375577 missense variant G/A snv 5
rs121913344
TP53
0.925 0.200 17 7673704 stop gained G/A;T snv 5
rs1057520010
XPO1
0.882 0.200 2 61492336 missense variant T/A;G snv 5
rs121913333
APC
0.882 0.120 5 112838220 stop gained C/A;T snv 6
rs1057519725
KRAS
0.851 0.320 12 25225627 missense variant G/A snv 7.0E-06 6
rs1057519732
MAP2K1
0.827 0.160 15 66436824 missense variant C/A;T snv 6
rs397516792
MAP2K1
0.827 0.280 15 66436825 missense variant C/A;G;T snv 6
rs764918809
MDM2
0.827 0.160 12 68839337 missense variant T/C snv 4.0E-06 6
rs10808555
PCAT1 ; POU5F1B ; CASC8
0.925 0.080 8 127397266 intron variant G/A snv 0.65 6
rs1057519931
PIK3CA
0.827 0.160 3 179199141 missense variant G/C snv 6
rs1057519962
SMAD4
0.827 0.160 18 51067035 missense variant G/A;T snv 6
rs719725 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 7
rs121913361
BRAF
0.807 0.280 7 140753349 missense variant C/A;G;T snv 7
rs1057519882
CDKN2A
0.807 0.200 9 21974678 missense variant C/A snv 7
rs770248150
KRAS
0.807 0.240 12 25225713 missense variant T/A;G snv 4.0E-06 7
rs1057519917
MTOR
0.807 0.160 1 11124517 missense variant A/G;T snv 7
rs749415085
PIK3CA
0.807 0.160 3 179198937 missense variant C/A;G;T snv 7
rs772110575
PIK3CA
0.807 0.160 3 179198938 missense variant G/A;T snv 4.0E-06 7