Disease: Stomach Carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10116253 0.851 0.120 9 117702042 upstream gene variant T/C snv 0.28 4
rs10484761 0.807 0.080 6 40834522 intergenic variant T/C snv 0.31 7
rs10811474 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 11
rs10983755 0.790 0.320 9 117702392 upstream gene variant G/A snv 3.2E-02 7
rs11040869 0.925 0.080 11 1263382 downstream gene variant G/A snv 1.8E-02 2
rs11088680 0.925 0.080 21 13514758 upstream gene variant A/G snv 0.30 2
rs12083239 0.925 0.080 1 39985357 intergenic variant G/A;C snv 3
rs12155758 0.882 0.080 8 142684467 upstream gene variant G/A snv 0.23 3
rs12521436 0.827 0.120 5 143438042 upstream gene variant G/A snv 0.21 5
rs12615966 0.882 0.080 2 104762499 upstream gene variant C/T snv 0.14 3
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs1887427 0.925 0.080 9 4979730 upstream gene variant A/G snv 0.21 2
rs1892901 0.925 0.080 11 65903422 upstream gene variant G/A snv 9.5E-03 2
rs1917799 0.851 0.120 10 49542929 upstream gene variant A/C snv 0.25 4
rs1924966 0.807 0.080 13 72432915 intergenic variant T/G snv 0.33 6
rs2178146 0.827 0.080 16 86430089 downstream gene variant T/C snv 0.31 8
rs26160 0.925 0.080 5 145353893 intron variant T/C snv 4.5E-03 2
rs2689154 0.882 0.080 1 238745053 intergenic variant C/A;G;T snv 3
rs36012910 0.925 0.080 2 25345310 upstream gene variant A/C;G snv 2
rs398652 0.752 0.240 14 56058851 intergenic variant G/A snv 0.24 10
rs4145643 0.925 0.080 10 60803097 regulatory region variant G/C;T snv 2
rs4460629 0.882 0.080 1 155162859 intergenic variant T/C snv 0.56 4
rs4733616 0.882 0.120 8 127649850 intergenic variant C/A;T snv 3
rs4912913 0.827 0.120 5 143438741 upstream gene variant T/C snv 0.48 5