Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134