Disease: Primary malignant neoplasm of lung
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10508266 0.882 0.080 10 3797822 intergenic variant G/A;T snv 3
rs10512948 0.882 0.080 5 8233238 intron variant T/C snv 0.15 3
rs10811474 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 11
rs117781739 0.882 0.080 16 47835114 intron variant G/A;T snv 3
rs11878644 0.882 0.080 19 45373709 upstream gene variant T/C snv 0.53 3
rs12521436 0.827 0.120 5 143438042 upstream gene variant G/A snv 0.21 5
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs13162612 0.882 0.080 5 8042908 intergenic variant A/G snv 5.1E-02 3
rs1454694 0.827 0.080 4 181276794 intergenic variant T/C snv 0.20 5
rs1560642 0.882 0.080 5 148888172 intergenic variant T/C;G snv 3
rs1663689 0.882 0.080 10 8983232 intergenic variant T/C snv 0.25 3
rs1814343 0.882 0.080 11 129695357 regulatory region variant C/T snv 0.22 3
rs1862214 0.882 0.080 19 32544943 intergenic variant G/A;C snv 4
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 12
rs2069514 0.807 0.160 15 74745879 upstream gene variant G/A snv 0.13 9
rs2736107 0.882 0.080 5 1297739 upstream gene variant C/T snv 0.23 3
rs2736108 0.807 0.160 5 1297373 upstream gene variant C/T snv 0.24 6
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 9
rs2808630 0.742 0.240 1 159711078 downstream gene variant C/T snv 0.77 13
rs2924471 0.882 0.080 5 8055148 intergenic variant T/C snv 0.15 3
rs35755165 0.882 0.080 19 40840084 intron variant A/C;G snv 5
rs36115365 0.807 0.160 5 1313127 upstream gene variant G/A;C;T snv 7
rs3742038 0.882 0.080 12 120371388 non coding transcript exon variant A/G snv 0.16 3
rs3856776 0.882 0.080 3 189580619 intergenic variant C/A;G;T snv 3
rs4105144 0.827 0.160 19 40852719 intron variant T/C snv 7