Disease: Adenocarcinoma of pancreas
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519944
POLE
0.882 0.160 12 132676599 missense variant G/A snv 5
rs1057519919
MYCNOS ; MYCN
0.851 0.160 2 15942195 missense variant C/T snv 5
rs1057519738
MIR4728 ; ERBB2
0.790 0.160 17 39725079 missense variant G/A snv 4.0E-06 7
rs1057519943
POLE
0.790 0.160 12 132676598 missense variant G/C;T snv 5
rs1057519936
PIK3CA
0.776 0.200 3 179234284 missense variant A/G;T snv 11
rs1057519937
PIK3CA
0.776 0.200 3 179234285 missense variant T/C snv 11
rs1057519977
TP53
0.763 0.360 17 7675189 missense variant G/C snv 13
rs1057519978
TP53
0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
rs121913413
CTNNB1
0.763 0.240 3 41224634 missense variant C/A;T snv 9
rs765848205
TP53
0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs1057519886
CTNNB1
0.752 0.240 3 41224609 missense variant T/A;C;G snv 11
rs587782664
TP53
0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 14
rs876660333
TP53
0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs587777790
PIK3CA
0.732 0.280 3 179199690 missense variant G/A snv 12
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 15
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
rs121913412
CTNNB1
0.724 0.280 3 41224633 missense variant A/C;G;T snv 10
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs1057520007
TP53
0.701 0.440 17 7674917 missense variant T/A;C;G snv 17
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 14
rs730882005
TP53
0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 18
rs1057520002
TP53
0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 21