Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10199605
LINC00299
1.000 0.120 2 8354967 intron variant G/A snv 0.26 1
rs10214237 1.000 0.120 5 35883632 downstream gene variant T/C snv 0.21 1
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 2
rs10738626 1.000 0.120 9 22373458 intergenic variant C/G;T snv 1
rs10791824
OVOL1-AS1 ; OVOL1
0.882 0.160 11 65791795 intron variant A/G;T snv 3
rs10888499 1.000 0.120 1 152560266 intergenic variant C/A;T snv 1
rs10995251
LOC105378327 ; ZNF365
1.000 0.120 10 62638706 intron variant C/T snv 0.29 1
rs11205006 1.000 0.120 1 152467700 intergenic variant A/T snv 0.72 1
rs112111458 0.925 0.120 2 70872975 intergenic variant A/G snv 0.16 1
rs12081541 0.925 0.160 1 152468890 intergenic variant T/C snv 8.9E-02 2
rs12130219
LOC112268240 ; PUDPP2 ; FLG-AS1
0.925 0.120 1 152189630 non coding transcript exon variant A/G snv 0.23 2
rs12144049 1.000 0.120 1 152468434 intergenic variant C/G;T snv 1
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 2
rs12188917
TH2LCRR ; IL13
1.000 0.120 5 132655393 intron variant T/C;G snv 1
rs12634229 0.882 0.120 3 112657461 intergenic variant T/C snv 0.15 1
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 4
rs1295686
TH2LCRR ; IL13
0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 3
rs13015714
IL18R1
0.882 0.200 2 102355405 intron variant G/T snv 0.77 2
rs13132933 0.925 0.200 4 122089432 upstream gene variant T/C snv 0.22 1
rs13199524
TNXB
0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 1
rs1343795
ZNF652
0.882 0.120 17 49334880 intron variant C/A snv 0.78 1
rs1384974 0.925 0.120 3 177009491 downstream gene variant T/C snv 9.6E-02 2
rs1444418 1.000 0.120 10 62800710 intron variant A/G snv 0.22 1
rs148203517
HLA-B ; MIR6891
1.000 0.120 6 31356323 missense variant G/A;T snv 1