Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs11203203 0.807 0.240 21 42416077 intron variant G/A snv 0.28 9
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs2237892 0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs3134069 0.776 0.320 8 118952749 upstream gene variant A/C snv 9.6E-02 11
rs3134945 0.827 0.240 6 32178715 intron variant C/A snv 0.18 6
rs3217992 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 22
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs497309 0.882 0.240 6 31924707 intron variant A/C;G snv 5
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs8192284 0.724 0.720 1 154454494 missense variant A/C;T snv 19