Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 3
rs17582416 0.882 0.160 10 34998722 regulatory region variant T/G snv 0.31 3
rs7765379 0.827 0.280 6 32713151 upstream gene variant T/G snv 0.10 3
rs1063355
HLA-DQB1-AS1 ; HLA-DQB1
0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56 2
rs2315008
ZGPAT
0.925 0.120 20 63712604 intron variant T/G snv 0.70 2
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 2
rs17234657 0.882 0.120 5 40401407 intergenic variant T/G snv 0.14 1
rs17309827
SLC22A23
1.000 0.040 6 3433084 intron variant T/G snv 0.30 1
rs17695092
CPEB4
1.000 0.040 5 173910850 intron variant T/G snv 0.22 1
rs1819333 1.000 0.040 6 166960059 upstream gene variant T/G snv 0.57 1
rs3135503
CYLD
1.000 0.040 16 50757339 intron variant T/G snv 0.32 1
rs4372078
TNFSF15
1.000 0.040 9 114801407 intron variant T/G snv 0.78 1
rs72981516
FCHSD2
1.000 0.040 11 72959855 intron variant T/G snv 6.2E-05 1
rs751271
NOD2
1.000 0.040 16 50717264 intron variant T/G snv 0.61 1
rs751919
LOC102724907 ; MIR3181 ; CYLD
1.000 0.040 16 50741834 intron variant T/G snv 0.35 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs11742570 0.925 0.040 5 40410482 upstream gene variant T/C;G snv 2
rs4780355
SOCS1 ; RMI2 ; LOC105371082
0.882 0.120 16 11254001 intron variant T/C;G snv 2
rs8049439
ATXN2L
0.925 0.120 16 28826194 intron variant T/C;G snv 0.38 2
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 1
rs6716753
SP140
1.000 0.040 2 230232414 intron variant T/C;G snv 1
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10