Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9833888 1.000 0.080 3 100004736 intron variant G/T snv 0.18 1
rs9837602 1.000 0.080 3 100105841 intron variant G/A snv 0.18 1
rs181337095 1.000 0.080 15 100366889 intergenic variant G/A snv 1
rs612683 1.000 0.080 1 100414772 intron variant A/T snv 0.38 1
rs17094222 0.925 0.080 10 100635683 intergenic variant T/C snv 0.17 1
rs575018 1.000 0.080 5 101043689 intergenic variant C/G;T snv 1
rs514192 1.000 0.080 8 101466731 intron variant A/G;T snv 1
rs71559437 1.000 0.080 7 101909160 intron variant G/A snv 8.5E-02 1
rs6214 0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 1
rs369574511 1.000 0.080 7 102478605 intron variant T/C snv 1
rs3774937 0.776 0.280 4 102513096 intron variant T/C snv 0.26 5
rs57237364 1.000 0.080 7 102824786 intron variant TTTTTTTTTTT/-;T;TTTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTTT delins 1
rs4919687 0.742 0.160 10 102835491 non coding transcript exon variant G/A snv 0.25 9
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs281439 0.925 0.080 19 10289434 upstream gene variant G/C;T snv 1
rs12548629 0.776 0.120 8 103189173 intron variant C/T snv 0.24 10
rs6946892 1.000 0.080 7 103251337 intron variant T/C;G snv 1
rs280519 0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 1
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs7907606 0.790 0.120 10 103920874 upstream gene variant T/G snv 0.26 5
rs4742903 1.000 0.080 9 104094512 intron variant G/A;C snv 1
rs9348512 1.000 0.080 6 10456473 non coding transcript exon variant C/A snv 0.34 1
rs1092913 0.925 0.080 5 10467590 intron variant G/A snv 0.19 1
rs10623258 1.000 0.080 14 104745924 non coding transcript exon variant -/TT ins 0.56 1