Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs543293 0.925 0.080 11 86109035 regulatory region variant A/G snv 0.72 3
rs62117160 0.925 0.120 19 44728895 upstream gene variant G/A;T snv 3
rs75627662 1.000 0.080 19 44910319 non coding transcript exon variant C/T snv 0.17 3
rs759819 1.000 0.080 19 54304302 intron variant C/G;T snv 3
rs823118 0.925 0.080 1 205754444 upstream gene variant C/A;T snv 3
rs9877502 0.925 0.080 3 190951729 intergenic variant G/A snv 0.40 3
rs10222981 0.925 0.080 4 6759326 upstream gene variant G/T snv 0.14 2
rs10792832 1.000 0.080 11 86156833 downstream gene variant A/G snv 0.70 2
rs1163763 0.925 0.120 12 17567834 intron variant G/T snv 0.24 2
rs117905930 1.000 0.080 9 88973603 intron variant C/A;T snv 2
rs11894266 1.000 0.080 2 169780132 downstream gene variant C/T snv 0.45 2
rs12805422 1.000 0.080 11 45818338 intron variant G/A snv 0.42 2
rs141622900 1.000 0.080 19 44923535 upstream gene variant G/A snv 5.9E-02 2
rs147906088 1.000 0.080 7 54496119 intergenic variant C/A;T snv 2
rs17090219 0.925 0.080 18 56523802 intergenic variant T/C snv 7.4E-02 2
rs1992269 0.925 0.080 18 1872316 intron variant C/T snv 0.24 2
rs2525776 0.925 0.080 7 81272303 intergenic variant C/T snv 0.19 2
rs2582367 1.000 0.080 8 27622508 regulatory region variant C/T snv 0.64 2
rs28868104 1.000 0.080 3 104241993 intergenic variant C/T snv 0.17 2
rs365521 0.925 0.080 17 62944934 intron variant A/G snv 0.62 2
rs376465 0.925 0.080 19 22158230 intergenic variant T/C snv 0.46 2
rs4576506 0.925 0.120 9 31546474 intergenic variant A/G snv 0.91 2
rs4803770 0.925 0.120 19 44924096 upstream gene variant C/G snv 0.33 2
rs498055 0.925 0.080 10 95595157 non coding transcript exon variant C/A;G;T snv 0.39 2
rs58826447 1.000 0.080 19 44825122 downstream gene variant T/A;G snv 2