Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs10488631 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 5
rs2856683 0.827 0.320 6 32687441 regulatory region variant T/A;C;G snv 0.25 4
rs3135363 0.776 0.360 6 32421871 intergenic variant A/G snv 0.24 4
rs9357152 0.827 0.240 6 32697183 regulatory region variant A/G snv 0.24 4
rs9303277 0.790 0.240 17 39820216 intron variant C/T snv 0.52 4
rs6421571 0.851 0.200 11 118873063 intergenic variant T/A;C snv 3
rs12924729 0.882 0.200 16 11093926 intron variant G/A snv 0.34 2
rs6974491 0.807 0.120 7 37334906 intron variant G/A snv 0.14 2
rs7208487 0.925 0.080 17 39387196 intron variant T/A;G snv 2
rs2293370 0.882 0.160 3 119501087 intron variant G/A snv 0.18 2
rs1800693 0.776 0.360 12 6330843 non coding transcript exon variant T/C snv 0.36; 4.0E-06 0.38 2
rs4979462 0.790 0.240 9 114804733 intron variant C/T snv 0.13 2
rs12531711 0.827 0.200 7 128977412 intron variant A/C;G snv 2
rs2395148 0.882 0.200 6 32353777 intron variant G/T snv 4.6E-02 2
rs11117432 0.851 0.200 16 85985665 upstream gene variant G/A snv 0.15 1
rs12134279 0.925 0.080 1 197812068 regulatory region variant C/T snv 0.17 1
rs4679904 0.925 0.080 3 160623108 intergenic variant C/G;T snv 1
rs860413 0.925 0.080 5 35942940 upstream gene variant A/C snv 0.23 1
rs968451 0.925 0.080 22 39274846 intron variant G/T snv 0.18 1
rs4938534 0.925 0.080 11 111404408 intron variant G/A snv 0.56 1
rs7665590 0.925 0.080 4 98875633 3 prime UTR variant T/C snv 0.56 1
rs8017161 0.925 0.080 14 103096858 intron variant G/A snv 0.38 1
rs6441286 0.925 0.080 3 160011091 intron variant T/G snv 0.36 1