Disease: Gastric Adenocarcinoma
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913469
ERBB2
0.763 0.240 17 39723966 missense variant TT/CC mnv 8
rs1057519932
PIK3CA
0.683 0.320 3 179234298 missense variant T/G snv 22
rs1057520003
TP53
0.695 0.320 17 7675996 missense variant T/G snv 20
rs1057519999
TP53
0.763 0.160 17 7674247 missense variant T/C;G snv 12
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 24
rs121913272
PIK3CA
0.752 0.400 3 179210192 missense variant T/C;G snv 11
rs121913470
ERBB2
0.776 0.200 17 39723967 missense variant T/C;G snv 7
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 17
rs730882026
TP53
0.742 0.440 17 7674256 missense variant T/C;G snv 12
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 17
rs753660142
TP53
0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 10
rs1057519937
PIK3CA
0.776 0.200 3 179234285 missense variant T/C snv 11
rs876660807
TP53
0.763 0.160 17 7674248 missense variant T/C snv 12
rs121913284
PIK3CA
0.776 0.160 3 179203765 missense variant T/A;G snv 10
rs786203071
TP53
0.776 0.240 17 7675181 missense variant T/A;G snv 8
rs1057519985
TP53
0.724 0.360 17 7673763 missense variant T/A;C;G snv 15
rs1057519991
TP53
0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 19
rs1057519996
TP53
0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 16
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 20
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 20
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
rs1057519890
ERBB2
0.807 0.200 17 39723966 missense variant T/A snv 7
rs1057519916
MTOR
0.882 0.160 1 11109320 missense variant T/A snv 4
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 16