Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4925 0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs2304277 0.776 0.280 3 9759396 non coding transcript exon variant G/A snv 0.26 8
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205