Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1801275
IL4R
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs555743307
IL4R
0.695 0.440 16 27342243 missense variant G/A;T snv 3.6E-05; 2.9E-04 20
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 11
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 6
rs6906021
HLA-DQB1-AS1
0.827 0.320 6 32658534 upstream gene variant T/C snv 0.47 6
rs6932730 0.925 6 31386405 upstream gene variant T/C snv 0.26 5
rs2427837
FCER1A
0.851 0.160 1 159288755 upstream gene variant G/A snv 0.20 5
rs447713
IL1RN
0.851 0.160 2 113130095 non coding transcript exon variant A/G snv 0.21 5
rs769790595
IL4R
0.827 0.120 16 27360785 missense variant G/A;C snv 2.0E-05; 4.0E-06 5
rs2289278
TSLP
0.827 0.200 5 111073450 5 prime UTR variant C/G snv 8.7E-02 5
rs10056340 0.925 0.080 5 110854353 intergenic variant T/G snv 0.31 3
rs2251746
FCER1A
0.882 0.120 1 159302270 intron variant T/C snv 0.20 3
rs13222905
GIMAP4
0.882 0.160 7 150566901 upstream gene variant G/A snv 0.15 3
rs6965571
GIMAP5 ; GIMAP1-GIMAP5
0.882 0.160 7 150737384 5 prime UTR variant G/A snv 0.18 3
rs3771175
IL1RL1 ; IL18R1
0.925 0.080 2 102343750 3 prime UTR variant T/A snv 0.18 3
rs4742170
LOC107987046 ; IL33
0.925 0.080 9 6242950 intron variant C/G;T snv 3
rs9865818
LPP
1.000 3 188354725 intron variant A/G snv 0.34 2
rs4410871
PVT1
0.925 0.080 8 127802783 intron variant T/C snv 0.74 2
rs17616434
TLR1
1.000 4 38811255 intron variant T/C snv 0.44 2