Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10941112 0.882 0.120 5 34004602 missense variant C/T snv 0.42 0.38 4
rs1268298845
APC
0.882 0.120 5 112780878 missense variant G/A snv 4.0E-06 4
rs4539 0.925 0.080 8 142915123 missense variant T/C snv 0.42 0.38 4
rs386352318 0.925 0.080 11 128911776 missense variant T/G snv 4
rs756363791 0.882 0.080 3 9756823 missense variant G/A snv 2.0E-05 4
rs61734277 0.882 0.080 6 10874672 missense variant A/C snv 9.1E-03 8.6E-03 5
rs1290398674 0.851 0.240 20 58854075 missense variant G/A;T snv 5
rs2959656 0.851 0.160 11 64804546 missense variant T/C snv 0.94 0.90 5
rs7131056 0.827 0.200 11 113459052 intron variant A/C snv 0.51 6
rs1057517457 0.851 0.120 1 45332804 frameshift variant GCCAGCCCAG/- delins 7.0E-06 6
rs10808555 0.925 0.080 8 127397266 intron variant G/A snv 0.65 6
rs386352352 0.851 0.080 19 14097604 missense variant A/C snv 6
rs121912535 0.827 0.240 2 48688427 missense variant A/C snv 6
rs719725 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 7
rs7968585 0.851 0.160 12 47838310 downstream gene variant C/G;T snv 7
rs2302615 0.807 0.120 2 10448012 intron variant C/T snv 0.31 7
rs121908874 0.807 0.080 14 81143584 missense variant T/C snv 7
rs7837328 0.882 0.120 8 127410882 intron variant A/G snv 0.52 8
rs386352319 0.827 0.080 11 128911724 missense variant G/A;C snv 8
rs5277 0.790 0.160 1 186679065 synonymous variant C/G;T snv 0.12; 8.0E-06 9
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 11
rs1799732 0.790 0.160 11 113475529 intron variant -/G delins 11
rs3842787 0.776 0.200 9 122371228 missense variant C/T snv 5.9E-02 8.5E-02 11
rs7873784 0.752 0.440 9 117716658 3 prime UTR variant G/A;C;T snv 11
rs1105879 0.790 0.240 2 233693556 missense variant A/C snv 0.35 0.34 11