Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16977008 1.000 0.080 17 71920339 intergenic variant T/C snv 0.32 1
rs16977009 1.000 0.080 17 71920383 intergenic variant C/A;T snv 1
rs17033015 1.000 0.080 4 102625147 intergenic variant A/C snv 0.65 1
rs1859308 1.000 0.080 16 27386677 intergenic variant A/G snv 0.88 1
rs2168809 1.000 0.080 3 88328596 intergenic variant T/C snv 0.54 1
rs2422239 1.000 0.080 2 118271503 intergenic variant G/A snv 0.49 1
rs2422241 1.000 0.080 2 118285460 intergenic variant G/A snv 0.47 1
rs2732649 1.000 0.080 17 46267444 non coding transcript exon variant T/G snv 0.14 1
rs2894450 1.000 0.080 2 222132385 intergenic variant G/A snv 0.56 1
rs35569035 1.000 0.080 17 39879371 downstream gene variant C/T snv 0.35 1
rs36038753 1.000 0.080 17 39879117 downstream gene variant G/T snv 0.39 1
rs3862738 1.000 0.080 13 42512771 intergenic variant G/A snv 0.22 1
rs4353811 1.000 0.080 3 88932057 intergenic variant T/C snv 0.44 1
rs4552364 1.000 0.080 3 88925713 intergenic variant C/T snv 0.44 1
rs4675369 1.000 0.080 2 203778471 upstream gene variant A/G snv 0.15 1
rs4793389 1.000 0.080 17 71921776 regulatory region variant C/A snv 0.32 1
rs4936443 1.000 0.080 11 118870155 regulatory region variant C/T snv 0.73 1
rs4936444 1.000 0.080 11 118872629 regulatory region variant T/C;G snv 1
rs4938572 1.000 0.080 11 118870222 regulatory region variant C/T snv 0.73 1
rs4952108 1.000 0.080 2 30206869 upstream gene variant C/A;T snv 1
rs4973341 1.000 0.080 2 227795646 intergenic variant C/T snv 0.67 1
rs526231 1.000 0.080 5 103345680 intergenic variant C/T snv 0.24 1
rs527420934 1.000 0.080 17 46260063 non coding transcript exon variant G/C snv 1
rs552419936 1.000 0.080 17 46236391 regulatory region variant G/A snv 1
rs55768522 1.000 0.080 9 114811940 intergenic variant G/A snv 4.3E-02 1