Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519754
AKT2
19 40236313 missense variant T/C snv 1
rs121913326
APC
5 112839729 stop gained G/T snv 1
rs121913328
APC
5 112839693 stop gained C/T snv 1
rs121913329
APC
5 112839726 stop gained C/T snv 1
rs121913462
APC
5 112839510 stop gained G/A;T snv 1
rs1801166
APC
0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 1
rs74535574
APC
5 112839879 stop gained C/A;T snv 1
rs869312784
APC
5 112838674 missense variant A/G snv 1
rs1057519760
EGFR
7 55160314 missense variant A/G snv 1
rs138551214
EPHB2
0.925 0.080 1 22909025 missense variant G/A snv 4.0E-06 1.4E-05 1
rs121913236
KRAS
0.882 0.160 12 25245321 missense variant G/C;T snv 1
rs2236225
MTHFD1
0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 1
rs1554774973
NTRK2
1.000 0.120 9 84955504 missense variant C/T snv 1
rs10808555
PCAT1 ; POU5F1B ; CASC8
0.925 0.080 8 127397266 intron variant G/A snv 0.65 1
rs1057519740
SMAD4
18 51065532 missense variant C/A snv 1
rs1057519741
SMAD4
18 51078417 missense variant G/T snv 1
rs863225349
APC
1.000 0.120 5 112839531 missense variant A/G snv 2
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 2
rs7837328
CASC8 ; PCAT1 ; POU5F1B
0.882 0.120 8 127410882 intron variant A/G snv 0.52 2
rs1057519725
KRAS
0.851 0.320 12 25225627 missense variant G/A snv 7.0E-06 2
rs1057519699
PIK3CA
3 179218315 missense variant G/A snv 2
rs1566734
PTPRJ
0.807 0.120 11 48123823 missense variant A/C snv 0.17 0.15 2
rs1057519739
SMAD4
1.000 0.080 18 51065518 missense variant G/A;C snv 2
rs121913327
APC
0.925 0.120 5 112839606 stop gained C/G;T snv 3
rs121913238
KRAS
0.732 0.240 12 25227343 missense variant G/C;T snv 3