Disease: ovarian neoplasm
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs1057519925
PIK3CA
0.683 0.560 3 179210291 missense variant G/A;C snv 25
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs1057519988
TP53
0.776 0.240 17 7673812 missense variant A/C;G;T snv 10
rs1057519995
TP53
0.807 0.240 17 7674200 missense variant T/A snv 9
rs1057520002
TP53
0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs121909231
PTEN
0.667 0.600 10 87961095 stop gained C/A;T snv 32
rs121913273
PIK3CA
0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs121913281
PIK3CA
0.623 0.520 3 179234296 missense variant C/T snv 37
rs121913286
PIK3CA
0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913400
CTNNB1
0.683 0.360 3 41224610 missense variant C/A;G;T snv 26
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 22
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 22
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs397517201
PIK3CA
0.732 0.240 3 179218307 missense variant A/C;G;T snv 16
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 16
rs730882025
TP53
0.724 0.360 17 7674885 missense variant C/A;G;T snv 21
rs730882026
TP53
0.742 0.440 17 7674256 missense variant T/C;G snv 15