Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs11196067 0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1205454520 0.763 0.120 10 87864059 5 prime UTR variant -/G delins 7.2E-06 10
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913444 0.724 0.160 7 55191831 missense variant T/A;C;G snv 18
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs2243248
IL4
0.763 0.240 5 132672952 upstream gene variant T/A;C;G snv 9
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs4977756 0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs7003908 0.716 0.320 8 47858141 intron variant C/A snv 0.66 16
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
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
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144