Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 6
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs231804 0.925 0.200 2 203843923 intergenic variant C/T snv 0.60 3
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 3
rs4947296 0.851 0.440 6 31090401 intergenic variant T/A;C snv 3
rs1024161 0.925 0.160 2 203857029 intergenic variant T/A;C snv 2
rs1521 0.882 0.320 6 31382927 upstream gene variant C/T snv 0.74 2
rs6909253 0.925 0.200 6 30087866 intergenic variant G/A;T snv 2
rs9366076 0.925 0.200 6 166960220 upstream gene variant C/T snv 0.22 2
rs10197319 1.000 0.120 2 203898321 regulatory region variant G/A;T snv 1
rs10738760 0.807 0.320 9 2691186 regulatory region variant A/G snv 0.56 1
rs10908583 1.000 0.120 1 157671893 downstream gene variant C/T snv 0.57 1
rs1149386 1.000 0.120 1 160471451 TF binding site variant G/C snv 0.96 1
rs11571297 0.882 0.120 2 203880280 regulatory region variant T/C snv 0.44 1
rs11571302 0.925 0.200 2 203878211 downstream gene variant G/A;T snv 1
rs12743184 1.000 0.120 1 157784569 intergenic variant A/G snv 0.21 1
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 1
rs1456988 0.925 0.160 14 98021670 intergenic variant G/T snv 0.61 1
rs1610591 1.000 0.120 6 29710058 upstream gene variant A/G;T snv 1
rs2210911 1.000 0.120 1 157674077 downstream gene variant A/G snv 0.46 1
rs2240306 1.000 0.120 12 48040724 non coding transcript exon variant G/A snv 0.19 1
rs2254071 1.000 0.120 6 29838285 intergenic variant T/C;G snv 1
rs231726 0.790 0.200 2 203876143 downstream gene variant C/T snv 0.36 1