Disease: Serous cystadenocarcinoma ovary
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1057519879
PATL2 ; B2M
0.763 0.280 15 44711548 start lost T/C;G snv 10
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
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
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
rs876660807
TP53
0.763 0.160 17 7674248 missense variant T/C snv 12
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
rs1057520007
TP53
0.701 0.440 17 7674917 missense variant T/A;C;G snv 17
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
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 16
rs121913275
PIK3CA
0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29
rs149680468
FBXW7
0.742 0.320 4 152326137 missense variant G/A;C;T snv 12
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 14
rs28934573
TP53
0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 24
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 21