Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10509291 0.827 0.280 10 67875446 downstream gene variant T/A snv 7.1E-02 6
rs1073203 0.882 0.160 5 125983763 intron variant C/G snv 0.15 4
rs10757283 0.827 0.120 9 22134173 intergenic variant C/A;T snv 0.45 6
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs10818684 1.000 0.040 9 122407651 intron variant C/T snv 0.62 2
rs10885390 0.925 0.080 10 112881038 regulatory region variant T/A snv 0.30 3
rs10941191 1.000 0.040 5 34504693 intergenic variant C/A;T snv 3
rs11071657 1.000 0.040 15 62141763 regulatory region variant A/G snv 0.31 3
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs1206634 1.000 0.040 X 96302380 intron variant T/A;G snv 2
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12363572 0.925 0.080 11 68621498 upstream gene variant C/T snv 0.10 3
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs12513649 0.851 0.160 5 173045049 regulatory region variant C/G;T snv 6
rs1260236 1.000 0.040 9 6023030 intergenic variant A/G snv 2
rs12779790 0.882 0.120 10 12286011 intergenic variant A/G snv 0.17 5
rs12910524 1.000 0.040 15 101262360 intergenic variant T/A;C snv 2
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs13191445 0.925 0.120 6 26015261 upstream gene variant G/A snv 5.6E-02 4
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs1543654 1.000 0.040 21 34426752 upstream gene variant T/C snv 2
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19