Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66