Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1002481 0.882 0.080 6 111390819 intron variant T/A;G snv 3
rs10040363 0.882 0.080 5 83177826 intron variant A/G snv 0.50 3
rs10053847 0.882 0.080 5 35878038 3 prime UTR variant G/A snv 0.13 3
rs10054203 0.882 0.080 5 1279849 intron variant G/A;C;T snv 3
rs1014264982 0.882 0.080 19 3577038 missense variant G/A;C snv 6.8E-06 7.0E-06 3
rs10187911 0.882 0.080 2 50420809 intron variant C/A;G;T snv 3
rs10244817 0.882 0.080 7 124827416 intron variant T/C snv 0.22 3
rs10412613 0.882 0.080 19 52209575 intron variant G/A snv 0.63 3
rs1043973338 0.882 0.080 2 112830483 missense variant A/C snv 3
rs10487372 0.882 0.080 7 117560845 intron variant C/T snv 0.13 3
rs1049337 0.882 0.080 7 116560533 3 prime UTR variant C/T snv 0.25 3
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
rs10519203 0.851 0.080 15 78521704 intron variant G/A snv 0.67 3
rs1052486 0.851 0.200 6 31642909 missense variant A/G snv 0.51 0.44 3
rs1053566 0.882 0.080 19 7911079 missense variant C/T snv 3
rs1057519857 0.882 0.080 17 39724772 missense variant T/C snv 3
rs1057519984 0.882 0.080 17 7673777 missense variant G/C;T snv 3
rs1060503291
APC
0.882 0.080 5 112835135 missense variant C/T snv 3
rs1062980 0.827 0.080 15 78500185 3 prime UTR variant T/C snv 0.39 3
rs10750417 0.882 0.080 11 129612280 non coding transcript exon variant A/G;T snv 3
rs10853100 0.882 0.080 17 48525070 downstream gene variant T/C snv 0.41 3
rs11020802 0.882 0.080 11 94493959 upstream gene variant C/A;G;T snv 3
rs11072768 0.882 0.080 15 78637136 intron variant T/C;G snv 3
rs11090910 0.882 0.080 22 46111790 non coding transcript exon variant T/C snv 0.30 3