Disease: Adenocarcinoma of pancreas
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs764146326
TP53
0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 20
rs121913413
CTNNB1
0.763 0.240 3 41224634 missense variant C/A;T snv 9
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 21
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 15
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 18
rs1057519919
MYCNOS ; MYCN
0.851 0.160 2 15942195 missense variant C/T snv 5
rs121913281
PIK3CA
0.623 0.520 3 179234296 missense variant C/T snv 37
rs1057519738
MIR4728 ; ERBB2
0.790 0.160 17 39725079 missense variant G/A snv 4.0E-06 7
rs1057519944
POLE
0.882 0.160 12 132676599 missense variant G/A snv 5
rs587777790
PIK3CA
0.732 0.280 3 179199690 missense variant G/A snv 12
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
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
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 26
rs121913275
PIK3CA
0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 14
rs28934573
TP53
0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 24
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 23
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 22
rs876659802
TP53
0.732 0.440 17 7673787 missense variant G/A;C;T snv 15
rs121913283
PIK3CA
0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 14
rs371769427
U2AF1
0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06 9