Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17024869 0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs2071746 0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs28360071 0.708 0.240 5 83142293 intron variant GATGAGGAAACTAACTCTCAGTGGTGTTTA/- delins 0.48 18
rs7581886 0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs10506868 0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 16
rs12241008 0.716 0.160 10 112520943 intron variant T/C snv 0.13 16
rs7758229 0.732 0.120 6 160419220 intron variant G/A;T snv 16
rs822396 0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs9929218 0.732 0.160 16 68787043 intron variant G/A snv 0.28 16
rs28360317 0.716 0.280 5 83323739 intron variant -/CCT delins 0.24 15
rs3789243 0.776 0.120 7 87591570 intron variant A/G snv 0.50 14
rs4925386 0.776 0.080 20 62345988 intron variant T/C snv 0.56 14
rs10411210 0.742 0.160 19 33041394 intron variant C/T snv 0.22 13
rs2075686 0.742 0.240 5 83076927 intron variant C/T snv 1.7E-02 13
rs3813867 0.732 0.240 10 133526101 intron variant G/A;C snv 13
rs12733285 0.776 0.120 1 202952912 intron variant C/T snv 0.26 12
rs1342387 0.776 0.120 1 202945228 intron variant T/C snv 0.53 12
rs3757441 0.752 0.200 7 148827660 intron variant C/T snv 0.80 12
rs4143094 0.752 0.240 10 8047173 intron variant T/G snv 0.70 12
rs11874392 0.763 0.080 18 48926786 intron variant A/T snv 0.50 11
rs3116496 0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14 11
rs4791171 0.763 0.080 17 65545379 intron variant T/C snv 0.55 11
rs11196067 0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs2238126 0.776 0.080 12 11856807 intron variant A/G snv 0.18 10
rs454886
APC
0.763 0.280 5 112810420 intron variant A/G snv 0.26 10