Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1059288 0.882 0.320 6 33299895 3 prime UTR variant A/G snv 0.60 3
rs1063320 0.752 0.360 6 29830972 3 prime UTR variant C/G;T snv 12
rs1063355 0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56 5
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs12413578 0.882 0.160 10 9007290 intergenic variant C/G;T snv 4
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1738074 0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 9
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
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
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
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
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs2069705 0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
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
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11
rs2647044 0.882 0.240 6 32700133 intergenic variant G/A snv 0.10 3