Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11954856
APC
0.732 0.200 5 112751630 intron variant T/G snv 0.54 12
rs1761667
CD36
0.752 0.320 7 80615623 intron variant G/A snv 0.49 12
rs454886
APC
0.763 0.280 5 112810420 intron variant A/G snv 0.26 10
rs1984112
CD36
0.807 0.280 7 80613604 intron variant A/G snv 0.33 8
rs3838646
TTTY14
0.827 0.320 Y 18991182 intron variant CA/- del 8
rs9921222
AXIN1
0.925 0.120 16 325782 intron variant C/T snv 0.51 5
rs565453 0.882 0.160 5 112849696 intron variant A/C;G snv 4
rs1058818
TTTY14
0.925 0.200 Y 18991654 intron variant C/T snv 2
rs1058881
TTTY14
0.925 0.200 Y 18991085 intron variant C/T snv 2
rs7224837
AXIN2
0.925 0.200 17 65532005 intron variant G/A snv 0.89 2
rs1816769
APC
1.000 0.120 5 112774082 intron variant G/C snv 0.54 1
rs3846716
APC
1.000 0.120 5 112723897 intron variant A/G snv 0.52 1
rs150766139
NTHL1 ; TSC2
0.742 0.320 16 2046238 stop gained G/A snv 1.4E-03 1.4E-03 13
rs121913331
APC
0.851 0.120 5 112838934 stop gained C/A;T snv 8.0E-06 11
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
rs137854575
APC
0.807 0.120 5 112838399 stop gained C/A;G;T snv 4.7E-04 9
rs62619935
APC
0.807 0.120 5 112792446 stop gained C/G;T snv 4.0E-06 8
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
rs121913333
APC
0.882 0.120 5 112838220 stop gained C/A;T snv 6
rs137854580
APC
0.827 0.120 5 112827194 stop gained C/G;T snv 2.8E-05 6
rs2229992
APC
0.827 0.200 5 112827157 stop gained T/C;G snv 0.58 0.47 6
rs121913332
APC
0.925 0.120 5 112839942 stop gained C/G;T snv 4.0E-06 5