Disease: Malignant Uterine Corpus Neoplasm
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519874
RAC1
0.807 0.120 7 6387261 missense variant C/A;T snv 4
rs1057519948
RAC1
0.851 0.120 7 6387262 missense variant C/T snv 4
rs1057519920
NFE2L2
0.790 0.160 2 177234232 missense variant C/A;G;T snv 7
rs1057519938
PIK3CA
0.776 0.160 3 179203764 missense variant A/C;T snv 10
rs1057519939
PIK3CA
0.776 0.160 3 179203763 missense variant A/C snv 10
rs1057519947
PPP2R1A
0.790 0.160 19 52212730 missense variant G/A snv 9
rs1057519999
TP53
0.763 0.160 17 7674247 missense variant T/C;G snv 12
rs121913284
PIK3CA
0.776 0.160 3 179203765 missense variant T/A;G snv 10
rs759610249
FBXW7
0.790 0.160 4 152323032 missense variant C/T snv 8.0E-06 7.0E-06 8
rs786201419
TP53
0.790 0.160 17 7675180 missense variant C/A;T snv 8
rs876660807
TP53
0.763 0.160 17 7674248 missense variant T/C snv 12
rs1057519926
PIK3CA
0.776 0.200 3 179210293 missense variant A/T snv 10
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
rs1057519940
PIK3CA
0.752 0.200 3 179218308 missense variant G/T snv 13
rs121913399
CTNNB1
0.724 0.200 3 41224612 missense variant G/A;C snv 10
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 14
rs1057519921
NFE2L2
0.763 0.240 2 177234231 missense variant T/C snv 7
rs1057519927
PIK3CA
0.716 0.240 3 179218295 missense variant A/C;G;T snv 18
rs1057519933
PIK3CA
0.790 0.240 3 179199156 missense variant A/G snv 11
rs1057519934
PIK3CA
0.790 0.240 3 179199158 missense variant G/C snv 11
rs1057519935
PIK3CA
0.790 0.240 3 179199157 missense variant A/G snv 11
rs1057519941
PIK3CA
0.776 0.240 3 179203761 missense variant T/C;G snv 9
rs1057519989
TP53
0.732 0.240 17 7674233 missense variant C/A;G;T snv 15
rs28931589
CTNNB1
0.695 0.240 3 41224613 missense variant G/A;C;T snv 13