Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4819388
ICOSLG
0.790 0.240 21 44227538 3 prime UTR variant T/C 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
rs13010713
LINC01934
0.882 0.200 2 181131318 intron variant A/C;G snv 5
rs12928822
LOC105371082 ; RMI2
0.882 0.200 16 11310036 intron variant C/T snv 0.13 5
rs2816316
LOC105371664
0.882 0.200 1 192567683 intron variant C/A snv 0.79 5
rs13314993
LOC105377022
0.882 0.200 3 32973977 regulatory region variant G/C;T snv 5
rs1738074
LOC105378083 ; LOC107986664 ; TAGAP
0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 5
rs296547
MROH3P
0.882 0.200 1 200923009 intron variant T/C snv 0.53 5
rs17035378
PLEK ; LOC101927723
0.882 0.200 2 68371823 intron variant T/A;C snv 5
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 5
rs5754217
UBE2L3
0.925 0.120 22 21585386 intron variant G/T snv 0.31 5
rs2298428
YDJC
0.807 0.240 22 21628603 missense variant C/T snv 0.27 0.18 5
rs1250552
ZMIZ1
0.882 0.200 10 79298270 intron variant A/C;G snv 5
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs874040 0.925 0.160 4 26106575 downstream gene variant G/C snv 0.29 4
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 4
rs11676922
AFF3
0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs6859219
ANKRD55
0.925 0.160 5 56142753 intron variant C/A snv 0.20 4
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 4
rs864537
CD247
0.925 0.200 1 167442147 intron variant A/G snv 0.29 4
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 4
rs13315591
FAM107A ; LOC107984079
0.925 0.160 3 58571114 intron variant T/C snv 0.15 4
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 4
rs743777
IL2RB
0.827 0.200 22 37155567 intron variant A/G snv 0.36 4