Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2910032 1.000 0.040 5 153160794 intron variant C/T snv 0.52 2
rs7444191 1.000 0.040 5 152871873 intron variant G/A snv 0.54 2
rs12153740 1.000 0.040 5 152697204 intron variant T/A;C snv 1
rs10070616 5 153174146 intron variant C/T snv 0.33 1
rs1422560 5 153170644 intron variant T/A;G snv 1
rs1371063 1.000 0.040 5 153119610 intron variant T/C snv 0.49 1
rs1036605 1.000 0.040 5 153116973 intron variant A/G snv 0.33 1
rs17494099 1.000 0.040 5 153120463 intron variant A/G snv 0.11 1
rs2043847 1.000 0.040 5 153120252 intron variant G/C snv 0.53 1
rs17493476 1.000 0.040 5 153103246 intron variant T/G snv 0.14 1
rs6886088 1.000 0.040 5 153081231 intron variant C/T snv 0.12 1
rs4958608 1.000 0.040 5 153102787 intron variant G/A snv 0.12 1
rs6867434 1.000 0.040 5 153111474 intron variant T/G snv 0.48 1
rs7731686 1.000 0.040 5 153106846 intron variant A/T snv 0.36 1
rs17578145 1.000 0.040 5 153111905 intron variant A/C;G snv 1
rs17578068 1.000 0.040 5 153109462 intron variant T/A snv 0.11 1
rs17113985 1.000 0.040 5 153087229 intron variant G/A snv 2.5E-02 1
rs72804786 1.000 0.040 5 152938239 intron variant G/A snv 0.21 1
rs6868545 1.000 0.040 5 153115323 intron variant A/C snv 4.0E-02 1
rs113897692 1.000 0.040 5 152797226 intron variant A/G snv 0.20 1
rs111294930 1.000 0.040 5 152797561 intron variant A/G snv 0.20 1
rs76091702 1.000 0.040 5 153103403 intron variant C/A;T snv 3.9E-02 1
rs113568682 1.000 0.040 5 152920194 intron variant A/T snv 0.21 1
rs72799107 5 152673844 intron variant C/T snv 0.18 1
rs4958568 5 152636533 intron variant G/A snv 0.25 1