Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs11196067 0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
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
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs2243248
IL4
0.763 0.240 5 132672952 upstream gene variant T/A;C;G snv 9
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
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs4977756 0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205