Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs1927911 0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs4673 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36