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
rs17037102 0.807 0.240 4 106924637 missense variant C/A;T snv 0.15 6
rs7483 0.742 0.320 1 109737079 missense variant C/T snv 4.0E-06; 0.35 0.26 11
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
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs3206824 0.827 0.160 11 11964514 missense variant T/C snv 0.78 0.78 6
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2227284
IL4
0.732 0.480 5 132677033 intron variant T/C;G snv 12
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs10936599 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 32
rs6721961 0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
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
rs3021097 0.752 0.440 1 206773289 5 prime UTR variant A/G snv 10