Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1081432 1.000 0.080 2 6708412 intergenic variant T/C snv 1
rs1229544 1.000 0.080 7 97793192 intergenic variant C/T snv 4.6E-02 1
rs12309362 1.000 0.080 12 132466447 downstream gene variant G/A;T snv 1
rs1502174 1.000 0.080 3 135550249 intergenic variant A/G snv 0.46 1
rs2064836 1.000 0.080 X 92628018 downstream gene variant A/G;T snv 1
rs2198843 1.000 0.080 15 74708889 regulatory region variant C/G;T snv 1
rs2275959 1.000 0.080 8 37597541 non coding transcript exon variant G/A;C snv 1
rs3997872 1.000 0.080 6 32612840 intergenic variant T/A snv 0.14 1
rs405 1.000 0.080 7 91917013 intergenic variant G/A;C;T snv 1
rs584368 1.000 0.080 11 88232053 regulatory region variant C/T snv 0.70 1
rs6025211 1.000 0.080 20 56864307 intergenic variant C/G;T snv 1
rs6078460 1.000 0.080 20 12116249 intergenic variant A/C;G;T snv 1
rs649053 1.000 0.080 9 21387419 upstream gene variant A/G;T snv 1
rs7821974 1.000 0.080 8 37592483 downstream gene variant T/C snv 0.22 1
rs8113007 1.000 0.080 19 39252463 upstream gene variant A/T snv 0.29 1
rs878461 1.000 0.080 2 127415841 upstream gene variant T/C;G snv 0.11 1
rs9877457 1.000 0.080 3 135564539 intergenic variant A/G;T snv 1
rs9970827 1.000 0.080 1 185409746 regulatory region variant G/A snv 0.37 1
rs201159898 1.000 0.080 7 87549509 missense variant T/A;C snv 1.2E-05 4.9E-05 1
rs28364274 1.000 0.080 7 87504335 missense variant C/T snv 4.7E-03 4.6E-03 1
rs45456698 1.000 0.080 7 87504335 missense variant C/T snv 1
rs762334560
ALB
1.000 0.080 4 73404391 missense variant T/C snv 8.0E-06 7.0E-06 1
rs397514032
APC
1.000 0.080 5 112828923 frameshift variant A/- delins 1
rs2267401 1.000 0.080 22 38982116 intron variant T/A;G snv 1
rs760125354 1.000 0.080 22 38991371 stop gained G/C;T snv 1