Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs225014
DIO2
0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 1
rs1053874
DNASE1 ; TRAP1
0.851 0.240 16 3657746 missense variant G/A;T snv 0.36; 4.0E-06 1
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 1
rs1128334
ETS1
0.851 0.160 11 128459064 3 prime UTR variant C/T snv 0.11 1
rs13315591
FAM107A ; LOC107984079
0.925 0.160 3 58571114 intron variant T/C snv 0.15 1
rs11264799
FCRL3
0.851 0.240 1 157700967 upstream gene variant C/T snv 0.28 1
rs4675374
ICOS ; LOC101927840
0.882 0.200 2 203937855 intron variant T/C snv 0.65 1
rs4819388
ICOSLG
0.790 0.240 21 44227538 3 prime UTR variant T/C snv 1
rs743777
IL2RB
0.827 0.200 22 37155567 intron variant A/G snv 0.36 1
rs3811047
IL37
0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60 1
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 1
rs1059702
IRAK1
0.807 0.280 X 154018741 missense variant A/G snv 0.72 1
rs2004640
IRF5
0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 1
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 1
rs13119723
KIAA1109
0.807 0.280 4 122297158 intron variant A/G snv 0.10 1
rs13151961
KIAA1109
0.827 0.200 4 122194347 intron variant A/G snv 0.11 1
rs1678542
KIF5A
0.790 0.320 12 57574932 intron variant C/G snv 0.42 1
rs13010713
LINC01934
0.882 0.200 2 181131318 intron variant A/C;G snv 1
rs7523907
LOC101928512 ; CD247
1.000 0.080 1 167458010 non coding transcript exon variant C/A;T snv 1
rs10892258
LOC105369519
0.925 0.120 11 118709156 intron variant G/A snv 0.19 1
rs12928822
LOC105371082 ; RMI2
0.882 0.200 16 11310036 intron variant C/T snv 0.13 1
rs2816316
LOC105371664
0.882 0.200 1 192567683 intron variant C/A snv 0.79 1
rs13314993
LOC105377022
0.882 0.200 3 32973977 regulatory region variant G/C;T snv 1
rs212402
LOC105378083
1.000 0.080 6 159051263 intron variant G/A snv 0.66 1
rs212389
LOC105378083 ; LOC112267968
0.925 0.160 6 159068759 non coding transcript exon variant G/A snv 0.60 1