Disease: Malignant Uterine Corpus Neoplasm
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519900
FGFR2
0.882 0.120 10 121515259 missense variant C/T snv 3
rs121913474
FGFR2
0.790 0.200 10 121515260 missense variant A/G snv 3
rs1057519916
MTOR
0.882 0.160 1 11109320 missense variant T/A snv 4
rs1057519945
POLE
0.776 0.200 12 132673703 missense variant C/A;T snv 4
rs1057519862
ERBB2
0.851 0.160 17 39723405 missense variant G/A snv 5
rs1057519891
ERBB3
0.851 0.160 12 56088557 missense variant G/A;T snv 4.0E-06 5
rs1057519892
ERBB3
0.851 0.160 12 56088558 missense variant A/T snv 5
rs1057519915
MTOR
0.851 0.160 1 11109318 missense variant A/C snv 5
rs387906678
FGFR2
0.851 0.120 10 121515263 missense variant A/C;G snv 5
rs772110575
PIK3CA
0.807 0.160 3 179198938 missense variant G/A;T snv 4.0E-06 6
rs1057519738
MIR4728 ; ERBB2
0.790 0.160 17 39725079 missense variant G/A snv 4.0E-06 7
rs1057519890
ERBB2
0.807 0.200 17 39723966 missense variant T/A snv 7
rs121913470
ERBB2
0.776 0.200 17 39723967 missense variant T/C;G snv 7
rs749415085
PIK3CA
0.807 0.160 3 179198937 missense variant C/A;G;T snv 7
rs1057519893
ERBB3
0.790 0.160 12 56085070 missense variant G/A;T snv 8
rs121913365
BRAF
0.776 0.320 7 140753332 missense variant T/A;G snv 8
rs121913469
ERBB2
0.763 0.240 17 39723966 missense variant TT/CC mnv 8
rs786201419
TP53
0.790 0.160 17 7675180 missense variant C/A;T snv 8
rs786203071
TP53
0.776 0.240 17 7675181 missense variant T/A;G snv 8
rs1057519947
PPP2R1A
0.790 0.160 19 52212730 missense variant G/A snv 9
rs1057519926
PIK3CA
0.776 0.200 3 179210293 missense variant A/T snv 10
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
rs121913284
PIK3CA
0.776 0.160 3 179203765 missense variant T/A;G snv 10
rs121913399
CTNNB1
0.724 0.200 3 41224612 missense variant G/A;C snv 10