Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2094258 0.701 0.280 13 102844409 intron variant C/T snv 0.18 20
rs2854744 0.695 0.520 7 45921476 intron variant G/T snv 0.48 20
rs9651118 0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 19
rs2267437 0.724 0.320 22 41620695 intron variant C/A;G snv 19
rs10165970 0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10519097 0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs11943456 0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
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
rs2424913 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 18
rs28360071 0.708 0.240 5 83142293 intron variant GATGAGGAAACTAACTCTCAGTGGTGTTTA/- delins 0.48 18
rs6869366 0.701 0.280 5 83075927 intron variant T/G snv 9.2E-02 18
rs7581886 0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs3802842 0.695 0.280 11 111300984 intron variant C/A snv 0.71 17
rs4939827 0.708 0.160 18 48927093 intron variant T/A;C snv 16
rs8175347 0.708 0.400 2 233760234 intron variant TATA/-;TA;TATATA;TATATATA;TATATATATA;TATATATATATA delins 16
rs822396 0.732 0.400 3 186849088 intron variant G/A snv 0.81 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
rs4646536 0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 14
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
rs11954856
APC
0.732 0.200 5 112751630 intron variant T/G snv 0.54 12
rs12733285 0.776 0.120 1 202952912 intron variant C/T snv 0.26 12