Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs572527200 0.882 0.240 11 102875064 upstream gene variant T/C snv 4
rs9372120 0.851 0.280 6 106219660 intron variant T/G snv 0.16 5
rs549908 0.752 0.440 11 112150193 synonymous variant T/A;G snv 4.2E-06; 0.29 10
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs549858786 0.790 0.320 2 112836807 5 prime UTR variant T/A snv 10
rs367732974
F7
0.790 0.360 13 113105788 5 prime UTR variant G/A snv 8.9E-05 2.8E-05 9
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs881375 0.925 0.160 9 120890620 intron variant T/C snv 0.68 2
rs4505848 0.776 0.400 4 122211337 intron variant A/G snv 0.29 8
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs40401 0.776 0.440 5 132060785 missense variant C/T snv 0.29 0.33 8
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57