Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs2169059 1.000 0.080 4 117786035 intergenic variant C/A snv 0.56 1
rs2170568 1.000 0.080 8 129808129 intergenic variant T/A snv 0.15 1
rs2209907 1.000 0.080 9 80554440 regulatory region variant A/G snv 0.13 1
rs2423279 0.790 0.080 20 7831703 downstream gene variant T/C snv 0.29 1
rs367615 1.000 0.080 5 109613236 intergenic variant C/G;T snv 1
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 1
rs4140904 1.000 0.080 4 18314369 intergenic variant A/G snv 0.32 1
rs4574118 1.000 0.080 2 106331987 intergenic variant C/G snv 0.84 1
rs6469656 0.790 0.080 8 116635549 regulatory region variant G/A;C snv 1
rs6691170 0.776 0.080 1 221872104 intergenic variant G/T snv 0.34 1
rs7006896 1.000 0.080 8 129809948 regulatory region variant G/A snv 0.13 1
rs7553007 0.827 0.120 1 159728759 intergenic variant G/A snv 0.31 1
rs7667693 1.000 0.080 4 93944123 intergenic variant T/C snv 0.35 1
rs7988900 1.000 0.080 13 97826281 intergenic variant T/C snv 0.45 1