Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10826548 1.000 0.040 10 28966665 intergenic variant C/A snv 0.13 1
rs114181198 1.000 0.040 2 183618431 intergenic variant C/A snv 1
rs11514810 1.000 0.040 7 1388840 intergenic variant C/T snv 0.19 1
rs11564750 1.000 0.040 5 1447647 upstream gene variant G/C;T snv 6.6E-02 1
rs12036759 1.000 0.040 1 232789695 regulatory region variant A/G;T snv 1
rs12042052 1.000 0.040 1 232799973 upstream gene variant A/C;G;T snv 1
rs1330598 1.000 0.040 13 61358998 regulatory region variant T/A;C snv 1
rs142458453 1.000 0.040 12 31377392 downstream gene variant TAAATAAA/-;TAAA;TAAATAAATAAA;TAAATAAATAAATAAA;TAAATAAATAAATAAATAAA;TAAATAAATAAATAAATAAATAAA;TAAATAAATAAATAAATAAATAAATAAA delins 1
rs1427829 1.000 0.040 12 89366967 intron variant A/G snv 0.46 1
rs1464807 1.000 0.040 7 96733032 intergenic variant G/A;T snv 1
rs1517484 1.000 0.040 2 225373194 intergenic variant C/T snv 0.45 1
rs1592757 1.000 0.040 5 104554297 intron variant G/C snv 0.29 1
rs1616905 1.000 0.040 13 90718584 regulatory region variant T/C snv 1
rs17058466 1.000 0.040 18 75893390 intergenic variant G/A snv 2.6E-02 1
rs200508662 1.000 0.040 5 121055487 upstream gene variant C/G;T snv 1
rs2410116 1.000 0.040 8 13815938 intergenic variant A/G;T snv 1
rs28600876 1.000 0.040 11 69890712 intergenic variant G/C snv 0.31 1
rs4075163 1.000 0.040 9 88984188 intergenic variant C/A snv 0.43 1
rs4858241 1.000 0.040 3 20627579 intron variant T/G snv 0.31 1
rs56135409 1.000 0.040 3 20683524 intron variant C/A snv 0.27 1
rs5906754 1.000 0.040 X 49203767 upstream gene variant C/T snv 0.51 1
rs6686722 1.000 0.040 1 175764827 intergenic variant C/G;T snv 1
rs7181782 1.000 0.040 15 80394651 intron variant C/A;G snv 1
rs726967 1.000 0.040 4 55555546 downstream gene variant A/T snv 0.28 1
rs7403703 1.000 0.040 15 87839033 intergenic variant A/G snv 0.49 1