Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12928822
LOC105371082 ; RMI2
0.882 0.200 16 11310036 intron variant C/T snv 0.13 5
rs13010713
LINC01934
0.882 0.200 2 181131318 intron variant A/C;G snv 5
rs13098911
CCR3
0.882 0.200 3 46193709 intron variant C/G;T snv 5
rs13119723
KIAA1109
0.807 0.280 4 122297158 intron variant A/G snv 0.10 5
rs13151961
KIAA1109
0.827 0.200 4 122194347 intron variant A/G snv 0.11 5
rs13314993
LOC105377022
0.882 0.200 3 32973977 regulatory region variant G/C;T snv 5
rs17035378
PLEK ; LOC101927723
0.882 0.200 2 68371823 intron variant T/A;C snv 5
rs1738074
LOC105378083 ; LOC107986664 ; TAGAP
0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 5
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs2076530
TSBP1-AS1 ; BTNL2
0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 5
rs2298428
YDJC
0.807 0.240 22 21628603 missense variant C/T snv 0.27 0.18 5
rs2816316
LOC105371664
0.882 0.200 1 192567683 intron variant C/A snv 0.79 5
rs296547
MROH3P
0.882 0.200 1 200923009 intron variant T/C snv 0.53 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
rs5754217
UBE2L3
0.925 0.120 22 21585386 intron variant G/T snv 0.31 5
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 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
rs10892258
LOC105369519
0.925 0.120 11 118709156 intron variant G/A snv 0.19 4
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs11676922
AFF3
0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs13315591
FAM107A ; LOC107984079
0.925 0.160 3 58571114 intron variant T/C snv 0.15 4
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 4
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 4