Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912967
DCC
0.925 0.080 18 52906134 missense variant T/C snv 1
rs387906678
FGFR2
0.851 0.120 10 121515263 missense variant A/C;G snv 5
rs1057519900
FGFR2
0.882 0.120 10 121515259 missense variant C/T snv 3
rs1057519962
SMAD4
0.827 0.160 18 51067035 missense variant G/A;T snv 6
rs1057519952
RHOA
0.882 0.160 3 49375577 missense variant G/A snv 5
rs121913468
ERBB2
0.827 0.160 17 39724008 missense variant G/A;C;T snv 5
rs121913465
EGFR ; EGFR-AS1
0.763 0.160 7 55181312 missense variant G/T snv 3
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 1
rs121913228
CTNNB1
0.742 0.200 3 41224621 missense variant T/C;G snv 11
rs587782177
TP53
0.763 0.200 17 7674887 missense variant C/A;G;T snv 11
rs1057519889
EP300
0.807 0.200 22 41169525 missense variant G/A;T snv 6
rs756091827
MYC ; CASC11
0.851 0.200 8 127738435 missense variant C/G;T snv 6
rs1057519918
CASC11 ; MYC
0.851 0.200 8 127738390 missense variant C/T snv 5
rs1057519953
RHOA
0.807 0.200 3 49375576 missense variant C/A;T snv 5
rs750664148
CASC11 ; MYC
0.851 0.200 8 127738434 missense variant A/C;G snv 5
rs121913474
FGFR2
0.790 0.200 10 121515260 missense variant A/G snv 3
rs1057519927
PIK3CA
0.716 0.240 3 179218295 missense variant A/C;G;T snv 18
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 18
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 16
rs1057519989
TP53
0.732 0.240 17 7674233 missense variant C/A;G;T snv 15
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 14
rs587781991
TP53
0.724 0.240 17 7675208 missense variant C/A;T snv 14
rs867384286
FBXW7
0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs121913403
CTNNB1
0.683 0.240 3 41224622 missense variant C/A;G;T snv 13
rs765848205
TP53
0.763 0.240 17 7674253 missense variant A/C;G;T snv 12