Disease: Esophageal carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519889
EP300
0.807 0.200 22 41169525 missense variant G/A;T snv 6
rs1057519986
TP53
0.776 0.240 17 7673811 missense variant A/C;G snv 10
rs1057519987
TP53
0.776 0.280 17 7673810 missense variant A/C snv 10
rs1057519988
TP53
0.776 0.240 17 7673812 missense variant A/C;G;T snv 10
rs1057519997
TP53
0.776 0.320 17 7676037 missense variant A/C;G;T snv 9
rs121913465
EGFR ; EGFR-AS1
0.763 0.160 7 55181312 missense variant G/T snv 11
rs765848205
TP53
0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs1057520004
TP53
0.752 0.240 17 7674884 missense variant A/C;T snv 12
rs1057519883
CDKN2A
0.742 0.280 9 21971120 missense variant C/G;T snv 14
rs1057519896
FBXW7
0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs1057519992
TP53
0.742 0.400 17 7674890 missense variant T/A;C;G snv 14
rs149680468
FBXW7
0.742 0.320 4 152326137 missense variant G/A;C;T snv 15
rs587782664
TP53
0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 15
rs1057519989
TP53
0.732 0.240 17 7674233 missense variant C/A;G;T snv 17
rs375874539
TP53
0.732 0.320 17 7674237 missense variant G/A;C snv 15
rs867384286
FBXW7
0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs876659802
TP53
0.732 0.440 17 7673787 missense variant G/A;C;T snv 16
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 17
rs121912655
TP53
0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
rs587781991
TP53
0.724 0.240 17 7675208 missense variant C/A;T snv 17
rs730882025
TP53
0.724 0.360 17 7674885 missense variant C/A;G;T snv 21
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 19
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs985033810
TP53
0.724 0.280 17 7674232 missense variant C/A;G;T snv 16