Disease: Adenocarcinoma of lung (disorder)
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs4513061
AGBL1
0.807 0.080 15 86428401 intron variant G/A;T snv 6
rs3813565
LOC105370913 ; CHRNB4
0.851 0.080 15 78727268 splice region variant G/A;T snv 6
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1057520003
TP53
0.695 0.320 17 7675996 missense variant T/G snv 20
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 21
rs1057519996
TP53
0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 19
rs866775781
TP53
0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs587781991
TP53
0.724 0.240 17 7675208 missense variant C/A;T snv 17
rs1057519978
TP53
0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 16
rs1057519977
TP53
0.763 0.360 17 7675189 missense variant G/C snv 13
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 20
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
rs138729528
TP53
0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs786202962
TP53
0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 21
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 24
rs1057519991
TP53
0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 26
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 22