Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10511729 0.742 0.240 9 23557229 intron variant T/G snv 0.35 11
rs12683422 0.742 0.240 9 27969442 intron variant C/T snv 5.7E-02 11
rs16901904 0.790 0.160 8 127015257 intron variant T/C snv 0.27 7
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs2070584 0.790 0.200 X 47587120 intron variant T/G snv 0.44 8
rs2075685 0.724 0.320 5 83076846 intron variant G/A;T snv 14
rs2075686 0.742 0.240 5 83076927 intron variant C/T snv 1.7E-02 13
rs2107425 0.732 0.280 11 1999845 intron variant C/T snv 16
rs28360071 0.708 0.240 5 83142293 intron variant GATGAGGAAACTAACTCTCAGTGGTGTTTA/- delins 0.48 18
rs28360317 0.716 0.280 5 83323739 intron variant -/CCT delins 0.24 15
rs2854509 0.807 0.160 19 43570445 intron variant T/G snv 0.80 6
rs3136817 0.732 0.280 14 20456275 intron variant T/C snv 0.23 12
rs3731239 0.763 0.240 9 21974219 intron variant A/G snv 0.26 10
rs3740393 0.776 0.280 10 102876898 intron variant G/C;T snv 10
rs3757441 0.752 0.200 7 148827660 intron variant C/T snv 0.80 12
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs4957014 0.752 0.160 5 287899 intron variant T/G snv 0.74 11
rs6869366 0.701 0.280 5 83075927 intron variant T/G snv 9.2E-02 18
rs7003908 0.716 0.320 8 47858141 intron variant C/A snv 0.66 16
rs710886 0.763 0.160 8 127014615 intron variant C/T snv 0.37 9
rs762551 0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs7727691 0.763 0.200 5 83075876 intron variant C/T snv 0.32 9
rs8034191 0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs10811474 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 11
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134