Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10852936
ZPBP2
0.925 0.120 17 39875461 intron variant C/T snv 0.39 0.40 2
rs11078927
GSDMB
0.925 0.080 17 39908152 intron variant C/T snv 0.40 0.35 2
rs1295686
TH2LCRR ; IL13
0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 2
rs13076312
LPP
1.000 0.040 3 188371466 intron variant C/T snv 0.44 2
rs13091753
LPP
1.000 0.040 3 188396801 intron variant G/C;T snv 2
rs13093110
LPP
0.882 0.120 3 188407332 intron variant C/T snv 0.42 2
rs13330041
CLEC16A
1.000 0.120 16 10994951 intron variant G/A snv 0.25 2
rs13408569
IL1RL1 ; IL18R1
1.000 0.080 2 102338596 intron variant G/C snv 0.18 2
rs13408661
IL1RL1 ; IL18R1
1.000 0.080 2 102338622 intron variant G/A snv 0.18 2
rs1362348
IL18R1
1.000 0.080 2 102368164 intron variant C/G snv 0.45 2
rs1559810
LPP
1.000 0.040 3 188406566 intron variant C/A snv 0.36 2
rs17496549
HLA-DRA
6 32441931 intron variant C/T snv 0.10 2
rs17498196
LOC107987046 ; IL33
1.000 0.080 9 6237547 intron variant A/C;G snv 2
rs17616434
TLR1
1.000 4 38811255 intron variant T/C snv 0.44 2
rs17673553
CLEC16A
1.000 0.120 16 11148049 intron variant A/G snv 0.18 2
rs2066362
IL33
1.000 0.080 9 6219176 intron variant G/C;T snv 2
rs2069772
IL2
0.925 0.200 4 122451978 intron variant T/A;C snv 2
rs2294881
BTNL2 ; TSBP1-AS1
1.000 0.040 6 32399827 intron variant T/C snv 0.19 2
rs2294882
TSBP1-AS1 ; BTNL2
6 32399738 intron variant T/C snv 0.19 2
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 2
rs3755276
IL18R1
0.925 0.120 2 102361999 intron variant C/T snv 0.45 2
rs3771166
IL18R1
1.000 0.080 2 102369762 intron variant G/A;T snv 2
rs4851005
IL18R1
2 102395092 intron variant C/T snv 0.29 2
rs5029937
TNFAIP3
0.882 0.160 6 137874014 intron variant G/T snv 0.13 2
rs570963
TSBP1-AS1 ; TSBP1
1.000 0.120 6 32321817 intron variant A/G snv 0.21 2