Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11966332 1.000 0.120 6 31261924 intergenic variant C/T snv 0.14 1
rs12109285 1.000 0.120 5 21749239 intron variant T/A;C snv 1
rs12191360 1.000 0.120 6 32483584 intergenic variant C/A;T snv 1
rs1219414 1.000 0.120 11 121927189 intron variant G/A snv 0.31 1
rs1233665 1.000 0.120 6 28210734 intergenic variant T/A;C snv 1
rs12519788 1.000 0.120 5 30404961 intergenic variant G/A snv 0.35 1
rs12525220 1.000 0.120 6 32707693 upstream gene variant G/A snv 5.6E-02 1
rs12529514 1.000 0.120 6 14096427 regulatory region variant T/C snv 4.7E-02 1
rs12570744 1.000 0.120 10 6747501 intron variant C/T snv 0.20 1
rs12594231 1.000 0.120 15 31884101 intergenic variant T/C snv 0.45 1
rs1264344 1.000 0.120 6 30832800 upstream gene variant C/T snv 0.40 1
rs1264701 1.000 0.120 6 30098581 downstream gene variant G/T snv 0.16 1
rs1264708 1.000 0.120 6 30089377 intergenic variant A/G snv 0.21 1
rs12660883 1.000 0.120 6 30796643 downstream gene variant T/C snv 0.16 1
rs12873872 1.000 0.120 13 64366135 intergenic variant T/C snv 1
rs13020220 1.000 0.120 2 136062506 regulatory region variant C/T snv 1
rs13207033 1.000 0.120 6 137644281 intergenic variant G/A snv 0.24 1
rs13302591 1.000 0.120 9 130252358 intergenic variant G/A snv 0.14 1
rs13330176 1.000 0.120 16 85985481 upstream gene variant T/A snv 0.24 1
rs13385025 1.000 0.120 2 62233985 intergenic variant G/A;C snv 1
rs1340317 1.000 0.120 13 64356863 intergenic variant T/A snv 0.43 1
rs1340319 1.000 0.120 13 64376290 intergenic variant T/A;C snv 1
rs1367730 1.000 0.120 6 33090337 downstream gene variant C/T snv 0.33 1
rs1367731 1.000 0.120 6 33017422 intergenic variant C/G;T snv 1
rs141112 1.000 0.120 6 33036650 intergenic variant T/C snv 0.35 1