Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10434 0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs1550117 0.790 0.320 2 25343038 upstream gene variant A/G;T snv 11
rs1569686 0.752 0.400 20 32779273 intron variant G/A;C;T snv 15
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
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
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs4778889 0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79