Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17066873 0.851 0.040 13 76889874 non coding transcript exon variant T/C snv 5.4E-02 4
rs17154917 0.851 0.040 7 81207393 intergenic variant G/A;T snv 4
rs6586354 0.851 0.040 1 234897489 intron variant G/A snv 0.25 4
rs111365677 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 3
rs112538845 0.925 0.040 4 184084475 downstream gene variant C/T snv 1.7E-02 3
rs11591827 0.925 0.040 10 81128126 intergenic variant G/A snv 8.4E-02 3
rs12555870 0.925 0.040 9 23347726 intron variant A/G snv 0.36 3
rs1411216 0.925 0.040 9 24520196 intergenic variant A/G snv 0.73 3
rs143934587 0.925 0.040 20 19165806 intergenic variant G/A snv 9.1E-03 3
rs1548076 0.925 0.040 15 69934284 intergenic variant G/A snv 0.95 3
rs182377406 0.925 0.040 11 67449378 upstream gene variant A/G snv 4.5E-04 3
rs190783615 0.925 0.040 X 142772620 intergenic variant T/C snv 9.3E-03 3
rs1908557 0.925 0.040 4 89500202 intron variant T/C snv 0.31 3
rs201569130 0.925 0.040 6 1402916 intergenic variant GACA/- delins 1.1E-02 3
rs201921722 0.925 0.040 11 123679999 downstream gene variant -/A delins 9.2E-06 3
rs2979204 0.925 0.040 8 8441347 regulatory region variant T/C snv 0.34 3
rs34102224 0.925 0.040 8 5364506 downstream gene variant G/C snv 0.12 3
rs4761545 0.925 0.040 12 94032692 regulatory region variant G/T snv 0.56 3
rs56388524 0.925 0.040 5 45757459 intergenic variant C/A;T snv 2.0E-02 3
rs6546604 0.925 0.040 2 70415675 intron variant G/A;T snv 3
rs74860738 0.925 0.040 11 80671683 intergenic variant G/A snv 7.2E-02 3
rs7555693 0.925 0.040 1 106295917 intergenic variant G/A snv 0.45 3
rs75995702 0.925 0.040 11 42785177 intergenic variant C/G;T snv 3
rs77826363 0.882 0.040 6 1128802 intergenic variant G/T snv 2.2E-02 3
rs78087832 0.925 0.040 2 224600060 intergenic variant C/T snv 2.4E-03 3