Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs1800925
IL13 ; TH2LCRR
0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs17577
SLC12A5-AS1 ; MMP9
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 31
rs4833095
TLR1
0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 28
rs1555745467
CACNA1A
0.752 0.240 19 13262771 missense variant C/A snv 23
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
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 12
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 9
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 7
rs138726443
FLG ; FLG-AS1
0.790 0.200 1 152307547 stop gained G/A;C;T snv 2.8E-03; 4.0E-06; 1.6E-05 7
rs37973
GLCCI1 ; GLCCI1-DT
0.807 0.280 7 7968245 intron variant G/A;C snv 7
rs928413
IL33
0.807 0.120 9 6213387 upstream gene variant G/A;C snv 7
rs1438673 0.882 0.120 5 111131801 downstream gene variant C/T snv 0.61 4
rs3853750 0.882 0.160 5 110818610 intergenic variant T/C snv 0.30 4
rs10746463
CD55
0.851 0.200 1 207337251 missense variant G/A;T snv 4
rs17294280
SMAD3
0.882 0.120 15 67175947 intron variant A/G snv 0.19 4
rs17513503 0.882 0.120 5 110810746 intergenic variant C/A;G snv 3
rs10197862
IL18R1 ; IL1RL1
0.925 0.120 2 102350089 intron variant A/G snv 0.18 3
rs2069772
IL2
0.925 0.200 4 122451978 intron variant T/A;C snv 3
rs11049300 0.925 0.120 12 28042192 intergenic variant A/G snv 2.5E-02 2