Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 5
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 2
rs4833095
TLR1
0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 2
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 1
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 15
rs5743618
TLR1
0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 6
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 3
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 3
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 2
rs2856718 0.790 0.360 6 32702478 downstream gene variant C/T snv 0.34 2
rs3806933
TSLP
0.807 0.360 5 111071044 5 prime UTR variant C/A;T snv 0.40 1
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 1
rs11171739
ERBB3
0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49 4
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 3
rs3763313
BTNL2
0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 1
rs6906021
HLA-DQB1-AS1
0.827 0.320 6 32658534 upstream gene variant T/C snv 0.47 1
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 10
rs61839660
IL2RA
0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 9
rs9372120
ATG5
0.851 0.280 6 106219660 intron variant T/G snv 0.16 5
rs2305480
GSDMB
0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 4
rs1420101
IL1RL1 ; IL18R1
0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 3
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 2
rs17388568
ADAD1
0.827 0.280 4 122408207 intron variant G/A snv 0.20 2