Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1044129
AVEN ; RYR3
0.790 0.200 15 33866065 3 prime UTR variant A/G;T snv 9
rs28929495
EGFR
0.807 0.120 7 55174014 missense variant G/A;C;T snv 9
rs13254738
PRNCR1 ; CASC19 ; PCAT1
0.807 0.160 8 127092098 non coding transcript exon variant C/A;T snv 8
rs909797662
EGFR
0.790 0.120 7 55191837 missense variant G/A snv 8
rs773442580
EGF
0.851 0.080 4 109913367 missense variant T/C;G snv 4.0E-06 7
rs975263
MACC1
0.827 0.120 7 20158817 stop gained G/A;T snv 0.34 7
rs1131691029
TP53
0.827 0.160 17 7673794 missense variant C/G snv 6
rs1418586322
MLH1
0.827 0.160 3 37050495 missense variant C/G snv 4.0E-06 6
rs17878467
BIRC5
0.925 0.080 17 78214076 upstream gene variant C/G;T snv 6
rs35187787
CDH1
0.827 0.120 16 68822063 missense variant G/A;T snv 3.3E-03; 2.4E-05 6
rs121913314
SRC
0.851 0.120 20 37403359 stop gained C/T snv 5
rs1289280947
CDKN2A
0.851 0.080 9 21974571 missense variant C/T snv 4.0E-06 5
rs35301225
MIR34A ; MIR34AHG
0.882 0.080 1 9151743 mature miRNA variant C/A;T snv 5
rs4135113
TDG
0.925 0.080 12 103982915 missense variant G/A;C;T snv 4.7E-02 5
rs6918698
CCN2
0.851 0.200 6 131952117 intron variant G/A;C snv 5
rs1383147053
DLD
0.882 0.120 7 107901762 missense variant G/A snv 4
rs1450081432
PMS2
0.851 0.120 7 5987230 missense variant C/T snv 4.0E-06 4
rs3219145
PARP1
0.882 0.120 1 226363128 missense variant T/C;G snv 1.2E-02; 4.0E-06 4
rs756363791
OGG1
0.882 0.080 3 9756823 missense variant G/A snv 2.0E-05 4
rs910532454
CXCR4
0.882 0.080 2 136115453 missense variant C/A;T snv 4.0E-06 4
rs1017621656
TGFB1
0.925 0.080 19 41352923 missense variant A/C;G snv 1.9E-05 3
rs1057519822
MAP2K1
0.925 0.080 15 66481818 missense variant T/A snv 3
rs11986055
IKBKB
0.882 0.080 8 42277660 intron variant A/C;G snv 3
rs121913538
KRAS
0.882 0.080 12 25245328 missense variant C/A;G snv 3
rs1380087059
APC
0.882 0.160 5 112837749 missense variant G/C snv 4.0E-06 3