Disease: Carcinoma of lung
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1330189219
LTA ; LOC100287329 ; TNF
0.882 0.080 6 31573570 synonymous variant C/T snv 4.0E-06 5
rs3842
ABCB1
0.882 0.080 7 87504050 3 prime UTR variant T/C snv 0.16 5
rs5744724
POLK
0.882 0.080 5 75599649 3 prime UTR variant G/C snv 5.4E-02 5
rs2233947
PSORS1C2 ; PSORS1C1
0.851 0.080 6 31139278 non coding transcript exon variant C/T snv 9.3E-03 6
rs2352028
GPC5
0.851 0.080 13 91792975 intron variant C/G;T snv 6
rs3757328
ZNRD1 ; ZNRD1ASP
0.851 0.120 6 30060575 non coding transcript exon variant G/A snv 9.8E-02 6
rs3814058
NR1I2
0.851 0.120 3 119818444 3 prime UTR variant T/C snv 0.28 6
rs12415607
CASP7
0.827 0.160 10 113678445 upstream gene variant C/A snv 0.22 7
rs144779807
TERT
0.827 0.120 5 1268529 missense variant C/A;T snv 4.0E-06; 4.0E-05 7
rs1805076
PPP2R1B
0.851 0.120 11 111764842 missense variant C/T snv 6.5E-03 7.0E-03 7
rs2522137
MSI1
0.827 0.120 12 120342128 3 prime UTR variant T/A;C;G snv 7
rs28399433
CYP2A6
0.827 0.200 19 40850474 intron variant A/C;G;T snv 0.10; 4.4E-06 7
rs3212961
ERCC1
0.827 0.200 19 45419065 intron variant G/A;T snv 1.9E-04; 0.20 7
rs551060742
MSH2
0.827 0.120 2 47482929 stop gained C/T snv 8.4E-05 1.0E-04 7
rs74790047
CHD4
0.851 0.120 12 6601978 missense variant A/C;G snv 2.0E-05; 1.2E-04; 5.2E-03 1.7E-03 7
rs2230229
TNFRSF10A
0.807 0.120 8 23191779 missense variant C/T snv 0.88 0.86 8
rs25406
PCNA-AS1 ; PCNA
0.807 0.120 20 5118990 intron variant G/A snv 0.41 8
rs3793784
ERCC6
0.827 0.120 10 49539493 5 prime UTR variant G/C snv 0.30 8
rs3819102
ENOSF1
0.827 0.120 18 675307 intron variant A/G snv 4.5E-02 3.6E-02 8
rs6183
GHR
0.827 0.080 5 42718990 missense variant C/A snv 2.3E-03 7.4E-04 8
rs664143
C11orf65 ; ATM
0.807 0.160 11 108354934 3 prime UTR variant A/G;T snv 8
rs664677
ATM
0.807 0.160 11 108272455 intron variant C/A;T snv 0.65 8
rs748491031
EGFR
0.827 0.120 7 55200384 stop gained C/G;T snv 1.2E-05 8
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 9
rs1635498
EXO1
0.807 0.160 1 241881973 missense variant C/A;G;T snv 0.96 9