Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333051 1.000 0.080 9 22136490 regulatory region variant A/G;T snv 1
rs1358030 0.925 0.120 10 106363841 intergenic variant G/A snv 0.57 1
rs1370176 1.000 0.080 15 62105035 regulatory region variant G/A snv 0.31 1
rs1423096 0.925 0.080 19 7674291 upstream gene variant T/C snv 0.92 1
rs1424642 1.000 0.080 2 57069423 intergenic variant A/C snv 0.78 1
rs1436953 1.000 0.080 15 62121815 intergenic variant C/T snv 0.60 1
rs1436955 1.000 0.080 15 62112183 regulatory region variant C/T snv 0.30 1
rs1558317 1.000 0.080 7 15025939 intergenic variant T/A snv 0.55 1
rs1558318 1.000 0.080 7 15025987 intergenic variant A/T snv 0.55 1
rs16851688 1.000 0.080 1 177679735 intron variant C/T snv 0.11 1
rs16869786 1.000 0.080 8 102777227 regulatory region variant T/C snv 1.4E-02 1
rs16956487 1.000 0.080 18 47657525 intergenic variant G/A;C snv 1
rs17059209 1.000 0.080 8 28582425 intergenic variant G/A snv 4.8E-02 1
rs17791513 1.000 0.080 9 79290675 intergenic variant A/G snv 6.2E-02 1
rs17803219 1.000 0.080 9 4390752 upstream gene variant C/G snv 6.8E-02 1
rs1860316 1.000 0.080 17 70610175 intergenic variant G/A snv 0.68 1
rs1884609 1.000 0.080 20 44293488 intergenic variant C/T snv 7.3E-02 1
rs1974620 1.000 0.080 7 15025842 intergenic variant C/A;T snv 1
rs2014132 1.000 0.080 3 23192848 downstream gene variant C/G;T snv 2.8E-02 1
rs2166706 1.000 0.080 11 92958366 intergenic variant T/A;C snv 1
rs2191113 1.000 0.080 17 70651680 intergenic variant G/A;T snv 1
rs2191348 1.000 0.080 7 15024630 intergenic variant G/T snv 0.54 1
rs2215383 1.000 0.080 7 15023358 intergenic variant T/C snv 0.54 1
rs221900 1.000 0.080 14 71137637 downstream gene variant T/C snv 0.44 1
rs243019 1.000 0.080 2 60358671 intron variant T/A;C snv 0.46 1