Disease: Adenocarcinoma of lung (disorder)
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11375254
TP63
0.882 0.080 3 189625454 intergenic variant A/-;AA;AAA;AAAA delins 3
rs1057519928
PIK3CA
0.807 0.200 3 179221147 missense variant A/C snv 8
rs1057519987
TP53
0.776 0.280 17 7673810 missense variant A/C snv 10
rs1057519986
TP53
0.776 0.240 17 7673811 missense variant A/C;G snv 10
rs1057519927
PIK3CA
0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs1057519978
TP53
0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
rs1057519988
TP53
0.776 0.240 17 7673812 missense variant A/C;G;T snv 10
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs530941076
TP53
0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 21
rs587782289
TP53
0.752 0.240 17 7674257 missense variant A/C;G;T snv 15
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs765848205
TP53
0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 20
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 22
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs1057520004
TP53
0.752 0.240 17 7674884 missense variant A/C;T snv 12
rs115392158
HLA-B
0.708 0.280 6 31347004 intron variant A/G snv 17
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs147680653 0.708 0.280 6 29785031 intergenic variant A/G snv 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs75316749
LOC107986051
0.701 0.280 3 169043635 intergenic variant A/G snv 4.2E-02 18
rs876658657
MLH1
0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs1023835002
B2M ; PATL2
0.763 0.280 15 44711547 start lost A/G;T snv 10