Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 6
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 5
rs3129890 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 5
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 5
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 5
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 5
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs10806425
BACH2
0.851 0.280 6 90216893 intron variant C/A snv 0.33 5
rs13098911
CCR3
0.882 0.200 3 46193709 intron variant C/G;T snv 5
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 5
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 5
rs4675374
ICOS ; LOC101927840
0.882 0.200 2 203937855 intron variant T/C snv 0.65 5
rs4819388
ICOSLG
0.790 0.240 21 44227538 3 prime UTR variant T/C snv 5
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 5
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 5
rs13151961
KIAA1109
0.827 0.200 4 122194347 intron variant A/G snv 0.11 5
rs13010713
LINC01934
0.882 0.200 2 181131318 intron variant A/C;G snv 5
rs1701704
LOC105369781 ; IKZF4
0.851 0.200 12 56018703 intron variant T/G snv 0.25 5