Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
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
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62