Disease: Esophageal carcinoma
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 18
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 25
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs483352697
TP53
0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 17
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv 16
rs587782664
TP53
0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 14
rs730882005
TP53
0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs730882008
TP53
0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 22
rs730882025
TP53
0.724 0.360 17 7674885 missense variant C/A;G;T snv 14
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 19
rs80338963
SMAD4
0.776 0.280 18 51065548 missense variant C/A;G;T snv 11
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 19
rs985033810
TP53
0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs1057519896
FBXW7
0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 21
rs786202962
TP53
0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 17
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 18
rs1057519883
CDKN2A
0.742 0.280 9 21971120 missense variant C/G;T snv 11
rs121913281
PIK3CA
0.623 0.520 3 179234296 missense variant C/T snv 37
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 34
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37
rs121913273
PIK3CA
0.605 0.440 3 179218294 missense variant G/A;C snv 21
rs138729528
TP53
0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs28934574
TP53
0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 27