Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs1990760 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs237025 0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs8192284 0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs228648 0.776 0.360 1 7853370 missense variant G/A snv 0.51 0.52 13
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs11203203 0.807 0.240 21 42416077 intron variant G/A snv 0.28 9
rs11622435 0.827 0.120 14 81151652 intron variant G/A snv 4.7E-02 7
rs3765209 0.851 0.040 21 15417030 intron variant C/T snv 0.31 7
rs80356664 0.882 0.120 11 2160878 missense variant C/G;T snv 5
rs1228534100 1.000 0.040 12 120978892 missense variant G/A snv 7.0E-06 3