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 59
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 19
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
rs11071657 1.000 0.040 15 62141763 regulatory region variant A/G snv 0.31 2
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 11
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 6
rs12363572 0.925 0.080 11 68621498 upstream gene variant C/T snv 0.10 3
rs12513649 0.851 0.160 5 173045049 regulatory region variant C/G;T snv 5
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 4
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 22
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 7
rs1543654 1.000 0.040 21 34426752 upstream gene variant T/C snv 2
rs17700633 0.882 0.120 18 60262199 intergenic variant G/A snv 0.28 4
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 26
rs1800592 0.807 0.200 4 140572807 upstream gene variant T/C snv 0.40 8
rs181914932 1.000 0.040 20 45932640 non coding transcript exon variant T/C snv 1.6E-02 2
rs1967017 0.882 0.160 1 145711421 upstream gene variant A/G snv 0.43 2
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 6