Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10866713 1.000 0.080 5 159491886 intron variant G/A snv 0.16 1
rs11086996 1.000 0.080 20 46095024 upstream gene variant C/T snv 0.20 1
rs11129295 1.000 0.080 3 27747289 intergenic variant C/T snv 0.39 1
rs11256593 1.000 0.080 10 6075359 upstream gene variant C/T snv 0.40 1
rs12048904 1.000 0.080 1 100865980 intergenic variant T/C snv 0.48 1
rs12087340 1.000 0.080 1 85281310 intron variant C/T snv 8.4E-02 1
rs12296430 1.000 0.080 12 6394334 splice region variant G/C snv 0.16 1
rs13333054 1.000 0.080 16 85977427 intron variant C/A;T snv 1
rs1356122 1.000 0.080 3 154465773 intergenic variant G/A;C snv 1
rs1401884 1.000 0.080 16 85979945 intron variant G/C snv 0.18 1
rs1438131 1.000 0.080 2 23283911 regulatory region variant G/A snv 0.34 1
rs1610630 1.000 0.080 6 29761509 intron variant C/T snv 0.81 1
rs1611715 1.000 0.080 6 29861705 intron variant A/C snv 0.30 1
rs1633069 1.000 0.080 6 29756424 intron variant C/G snv 0.81 1
rs1633070 1.000 0.080 6 29756370 intron variant T/A;C snv 1
rs1694112 1.000 0.080 6 32681887 intergenic variant T/A;C snv 1
rs1737060 1.000 0.080 6 29765192 upstream gene variant G/C snv 0.79 1
rs1737068 1.000 0.080 6 29763146 non coding transcript exon variant C/A snv 0.81 1
rs1841770 1.000 0.080 3 148038899 intron variant G/T snv 0.64 1
rs1843938 1.000 0.080 7 3073400 intergenic variant G/A snv 0.42 1
rs201847125 1.000 0.080 7 50285971 intergenic variant C/T snv 1
rs2157082 1.000 0.080 6 32792937 intergenic variant G/A;C;T snv 1
rs2163226 1.000 0.080 2 43134117 upstream gene variant T/C snv 0.33 1
rs2182410 1.000 0.080 10 6080706 intergenic variant T/A;C snv 1
rs233100 1.000 0.080 1 85306326 intron variant G/A snv 0.40 1