Disease: Colorectal Carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10152518 0.790 0.080 15 67884824 intergenic variant G/A;T snv 9
rs1035209 0.790 0.080 10 99585609 intergenic variant C/T snv 0.15 9
rs10821907 0.776 0.080 10 50888694 upstream gene variant C/T snv 0.20 12
rs10849438 0.790 0.080 12 6302870 intergenic variant T/G snv 1.0E-01 9
rs10951878 0.790 0.080 7 46887097 downstream gene variant C/A;T snv 9
rs11087784 0.776 0.080 20 7760329 intergenic variant A/G snv 0.13 10
rs11169572 0.790 0.080 12 50823107 downstream gene variant T/C snv 0.42 9
rs11190164 0.776 0.080 10 99591947 intergenic variant A/G snv 0.19 10
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 11
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs11610543 0.776 0.080 12 42740389 intergenic variant A/G;T snv 10
rs116353863 0.776 0.080 6 31042408 regulatory region variant T/C snv 2.2E-02 10
rs11903757 0.763 0.160 2 191722478 intron variant T/C snv 0.16 11
rs11907546 0.708 0.280 20 34131991 upstream gene variant C/A;T snv 17
rs11927424 0.790 0.080 3 88708681 intergenic variant A/G snv 0.39 9
rs12149163 0.776 0.080 16 86305709 upstream gene variant T/C snv 0.49 10
rs12447408 0.776 0.080 16 86218938 downstream gene variant G/A snv 0.21 10
rs12514517 0.776 0.080 5 40279974 intergenic variant G/A snv 0.21 10
rs12635946 0.790 0.080 3 113198071 intergenic variant C/T snv 0.32 9
rs12659017 0.790 0.080 5 126652483 intergenic variant G/A snv 0.27 9
rs12672022 0.776 0.080 7 45096824 downstream gene variant T/C snv 0.13 10
rs12708491 0.776 0.080 15 32700635 downstream gene variant G/A snv 0.33 10
rs12970291 0.763 0.120 18 75305279 intergenic variant G/A snv 2.8E-02 12
rs13086367 0.776 0.080 3 113185041 downstream gene variant A/G snv 0.38 10
rs13130787 0.790 0.080 4 93965880 intergenic variant T/C snv 0.35 9