Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6271 1.000 0.040 9 133657152 missense variant C/T snv 4.6E-02 4.8E-02 5
rs867671924 1.000 0.080 17 47292176 missense variant C/A snv 3
rs11229555 0.827 0.120 11 58641214 intron variant G/T snv 0.21 7
rs516246 0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 10
rs774229224
PLG
0.882 0.160 6 160706454 missense variant C/A;G snv 4.0E-06; 4.0E-06 6
rs1183194405
F2
0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 19
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs2066844 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 54
rs1799969 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
rs2066845 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 46
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs56149945 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131