Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2069772
IL2
0.925 0.200 4 122451978 intron variant T/A;C snv 2
rs250308
LOC102723444 ; TNFAIP8
1.000 0.040 5 119348602 intron variant T/A;C snv 2
rs2548992
IRF1-AS1
1.000 0.080 5 132472976 non coding transcript exon variant A/G;T snv 2
rs2766664
LOC101927770
1.000 0.080 20 53554702 intron variant A/G;T snv 2
rs3208007
RTEL1-TNFRSF6B ; RTEL1
1.000 0.080 20 63690935 synonymous variant T/C;G snv 0.74 2
rs4794820
LRRC3C
0.790 0.160 17 39933091 intron variant A/G;T snv 2
rs4850808 2 197711418 intron variant T/A;C snv 2
rs6011033
RTEL1-TNFRSF6B ; RTEL1
20 63691346 intron variant A/G;T snv 2
rs659529 1.000 0.080 11 111566171 downstream gene variant T/A;C snv 2
rs7848215
IL33
0.925 0.080 9 6213468 upstream gene variant C/A;G;T snv 2
rs793607
DUBR
1.000 0.080 3 107340876 intron variant G/A;C snv 2
rs7936070 1.000 0.080 11 76582483 intergenic variant G/A;T snv 2
rs8043253
EXD1
1.000 0.080 15 41211532 intron variant C/A;G;T snv 2
rs869402
GSDMB
0.925 0.160 17 39911790 intron variant T/A;C snv 2
rs9273374
HLA-DQB1-AS1
1.000 0.080 6 32658837 upstream gene variant A/G;T snv 2
rs950881
IL18R1 ; IL1RL1
1.000 0.120 2 102316052 intron variant G/A;T snv 2
rs1008723
GSDMB
0.925 0.160 17 39910014 intron variant G/C;T snv 1
rs1048990
PSMA6
0.790 0.280 14 35292469 5 prime UTR variant C/G;T snv 0.19; 4.0E-06 1
rs10760123
PHF19
9 120888256 intron variant T/A;G snv 1
rs10975488
IL33
9 6213829 upstream gene variant A/G;T snv 1
rs11217036 11 118805063 intergenic variant C/G;T snv 1
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv 1
rs11652139
PSMD3
17 39992780 intron variant G/A;C snv 1
rs12045923
PEX14
1 10583772 intron variant C/G;T snv 1
rs12479210
IL1RL1 ; IL18R1
1.000 0.080 2 102332701 intron variant C/A;T snv 1