Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
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
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs1550117 0.790 0.320 2 25343038 upstream gene variant A/G;T snv 11
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs555607708 0.667 0.360 22 28695869 frameshift variant G/- del 2.0E-03 1.8E-03 33
rs1569686 0.752 0.400 20 32779273 intron variant G/A;C;T snv 15
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105