Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs6734238 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 4
rs11676348 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 2
rs12413624 0.851 0.120 10 118519432 intergenic variant T/A snv 0.34 2
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 2
rs4242382 0.763 0.240 8 127505328 intergenic variant A/G;T snv 2
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 2
rs4779584 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 2
rs6687758 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 2
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 2
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 2
rs961253 0.732 0.240 20 6423634 intergenic variant C/A snv 0.34 2
rs1023890 1.000 0.080 4 117780291 intergenic variant G/A;C snv 1
rs1035209 0.790 0.080 10 99585609 intergenic variant C/T snv 0.15 1
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 1
rs11903757 0.763 0.160 2 191722478 intron variant T/C snv 0.16 1
rs11986063 1.000 0.080 8 116628076 regulatory region variant C/T snv 0.12 1
rs13130787 0.790 0.080 4 93965880 intergenic variant T/C snv 0.35 1
rs1321311 0.742 0.160 6 36655123 regulatory region variant C/A snv 0.28 1
rs140355816 0.790 0.080 8 116562277 intergenic variant C/G snv 9.8E-03 1
rs1583661 1.000 0.080 4 93941116 intergenic variant C/A;T snv 1
rs1870481 1.000 0.080 4 117741865 intergenic variant C/T snv 0.55 1
rs2128383 1.000 0.080 8 129808389 intergenic variant A/G snv 0.15 1