Disease: Adenocarcinoma of lung (disorder)
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs11907546 0.708 0.280 20 34131991 upstream gene variant C/A;T snv 17
rs138488080 0.882 0.120 6 29638984 upstream gene variant G/A snv 3
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs147527678 0.708 0.280 6 32699696 intergenic variant G/A;C snv 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
rs17391694 0.882 0.120 1 78157942 regulatory region variant C/T snv 7.8E-02 6
rs1862626 0.708 0.280 5 56737113 regulatory region variant G/T snv 0.68 17
rs186507655 0.708 0.280 1 1351675 upstream gene variant G/A snv 6.8E-03 17
rs4105144 0.827 0.160 19 40852719 intron variant T/C snv 7
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 8
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 12
rs72658409 0.925 0.080 9 22160088 regulatory region variant C/T snv 0.10 2
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs77468143 0.925 0.080 15 49084427 intergenic variant T/C;G snv 2
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 20
rs11610143
ACVR1B
0.925 0.080 12 51955287 intron variant C/G snv 0.18 2
rs4513061
AGBL1
0.807 0.080 15 86428401 intron variant G/A;T snv 6
rs595961
AGO1
0.807 0.160 1 35902179 intron variant A/G snv 0.30 0.37 6
rs71658797
AK5
0.925 0.080 1 77501822 intron variant T/A snv 7.3E-02 3
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv 7
rs1130409
APEX1
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs533748068
ARHGEF2 ; MIR6738
0.851 0.080 1 155950962 missense variant C/A;T snv 4.3E-06 7.0E-06 5
rs2290035
ARNTL
0.827 0.160 11 13386224 intron variant T/A snv 0.46 5