Disease: Malignant Uterine Corpus Neoplasm
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519989
TP53
0.732 0.240 17 7674233 missense variant C/A;G;T snv 15
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs121912657
TP53
0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 15
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
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
rs764146326
TP53
0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 20
rs866987936
FBXW7
0.752 0.240 4 152326214 missense variant C/A;G;T snv 12
rs985033810
TP53
0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs1057519874
RAC1
0.807 0.120 7 6387261 missense variant C/A;T snv 4
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
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 15
rs786201419
TP53
0.790 0.160 17 7675180 missense variant C/A;T snv 8
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 18
rs1057519946
PPP2R1A
0.732 0.280 19 52212729 missense variant C/G;T snv 17
rs121909224
PTEN
0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 35
rs1057519948
RAC1
0.851 0.120 7 6387262 missense variant C/T snv 4
rs121913281
PIK3CA
0.623 0.520 3 179234296 missense variant C/T snv 37
rs759610249
FBXW7
0.790 0.160 4 152323032 missense variant C/T snv 8.0E-06 7.0E-06 8
rs1057519929
PIK3CA
0.776 0.320 3 179199066 missense variant G/A snv 9
rs1057519942
PIK3CA
0.724 0.320 3 179203760 missense variant G/A snv 15