Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 8
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 8
rs2836878 0.851 0.200 21 39093608 intergenic variant G/A snv 0.23 4
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 4
rs6734238 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 4
rs12967135 18 60181790 intergenic variant G/A snv 0.24 3
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 3
rs10908713 1 159369769 intron variant T/C snv 0.47 2
rs11265174 1 159350569 intron variant T/A snv 0.35 2
rs11265196 1 159448422 intron variant G/A snv 0.47 2
rs12034864 1 159215190 regulatory region variant A/C;G;T snv 2
rs12047230 1 159509215 intergenic variant A/G snv 0.33 2
rs12072644 1 159245497 intergenic variant C/A;T snv 2
rs12739022 1 159689641 intergenic variant T/C snv 0.24 2
rs12741825 1 159700355 downstream gene variant C/T snv 0.24 2
rs12753193 1 65703996 non coding transcript exon variant G/A snv 0.58 2
rs12754915 1 159691079 intergenic variant T/C snv 0.25 2
rs1584252 1 159553838 upstream gene variant A/T snv 0.30 2
rs2794506 1 159615770 intergenic variant A/G snv 0.38 2
rs2794525 1 159632725 intergenic variant G/A;T snv 2
rs2808651 1 159636436 intergenic variant T/C snv 0.35 2
rs3027063 1 159216991 intergenic variant C/T snv 0.30 2
rs3845624 1 159248476 regulatory region variant A/C snv 0.57 2