Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113