Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11464691 17 40614389 intergenic variant -/A delins 0.68 1
rs10663129
RASA2
3 141602994 intron variant -/CT delins 0.29 1
rs111914382
TTC6
14 37627796 intron variant -/G delins 0.20 1
rs150254607 4 122532955 intergenic variant -/TAT ins 4.9E-02 1
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs4833103
TLR1
0.925 0.160 4 38813881 intron variant A/C snv 0.64 3
rs10455025
TSLP
1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24 2
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 2
rs56267605 1.000 0.080 4 122441954 intergenic variant A/C snv 0.29 2
rs848
IL13 ; TH2LCRR
0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67 2
rs227275
MANBA
4 102672741 intron variant A/C snv 0.55 1
rs2893907
ZNF365
10 62622599 intron variant A/C snv 0.65 1
rs3763313
BTNL2
0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 1
rs6815814
TLR1
1.000 0.080 4 38814717 intron variant A/C snv 0.43 1
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs7824394 8 80380364 intron variant A/C;T snv 1
rs479844 0.851 0.160 11 65784486 upstream gene variant A/G snv 0.44 5
rs17294280
SMAD3
0.882 0.120 15 67175947 intron variant A/G snv 0.19 4
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 4
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4
rs74847330
ARHGAP15
2 143074030 intergenic variant A/G snv 8.8E-02 4
rs2033784
SMAD3
1.000 0.080 15 67157322 intron variant A/G snv 0.35 3
rs36045143
LOC105371081 ; CLEC16A
1.000 0.080 16 11131109 intron variant A/G snv 0.18 3
rs10197862
IL18R1 ; IL1RL1
0.925 0.120 2 102350089 intron variant A/G snv 0.18 2
rs148505069 1.000 0.120 4 122496409 intergenic variant A/G snv 0.29 2