Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913286
PIK3CA
0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv 23
rs530941076
TP53
0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 21
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 20
rs753660142
TP53
0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs1057519946
PPP2R1A
0.732 0.280 19 52212729 missense variant C/G;T snv 18
rs985033810
TP53
0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs121913275
PIK3CA
0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 26
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 24
rs1057519932
PIK3CA
0.683 0.320 3 179234298 missense variant T/G snv 22
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 19
rs149680468
FBXW7
0.742 0.320 4 152326137 missense variant G/A;C;T snv 15
rs375874539
TP53
0.732 0.320 17 7674237 missense variant G/A;C snv 15
rs1057519896
FBXW7
0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 34
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 31
rs730882025
TP53
0.724 0.360 17 7674885 missense variant C/A;G;T snv 21
rs1057520002
TP53
0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs1057519996
TP53
0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 19
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs371769427
U2AF1
0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06 24
rs121909229
PTEN
0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 22