Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 15
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 10
rs4779584 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 8
rs2555639 0.851 0.080 4 174540379 non coding transcript exon variant T/C snv 0.38 7
rs719725 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 7
rs961253 0.732 0.240 20 6423634 intergenic variant C/A snv 0.34 7
rs1321311 0.742 0.160 6 36655123 regulatory region variant C/A snv 0.28 6
rs2853668 0.882 0.080 5 1299910 upstream gene variant G/T snv 0.33 5
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 5
rs2770150 0.925 0.080 9 117700861 upstream gene variant A/G snv 0.22 4
rs3093075 0.882 0.120 1 159710123 upstream gene variant G/T snv 0.13 4
rs6691170 0.776 0.080 1 221872104 intergenic variant G/T snv 0.34 4
rs6854845 0.827 0.080 4 74821455 intergenic variant G/T snv 0.13 4
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 4
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 3
rs12970291 0.763 0.120 18 75305279 intergenic variant G/A snv 2.8E-02 3
rs6687758 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 3
rs997476 0.882 0.080 4 102620848 downstream gene variant G/T snv 4.3E-02 3
rs11903757 0.763 0.160 2 191722478 intron variant T/C snv 0.16 2
rs1365611 0.925 0.080 4 174462542 intergenic variant C/T snv 0.28 2
rs16969681 0.776 0.080 15 32700910 downstream gene variant C/T snv 0.11 2
rs2332897 0.925 0.080 4 174465154 intergenic variant C/A;G snv 0.29 2
rs2965667 0.776 0.080 12 17291799 intergenic variant A/T snv 0.96 2
rs4813802 0.776 0.080 20 6718948 regulatory region variant T/G snv 0.28 2
rs6844282 0.925 0.080 4 174460480 regulatory region variant C/A;G snv 2