Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs71559680 0.827 0.120 6 21430497 intergenic variant TAG/CAT mnv 6
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs1569414
FAM118A
0.807 0.160 22 45331684 intron variant T/G snv 0.44 6
rs34779708
CREM
0.827 0.120 10 35177257 intron variant T/G snv 0.33 6
rs3776414
DAP
0.827 0.120 5 10689450 intron variant T/G snv 0.48 6
rs4243971 0.827 0.120 20 32261714 intergenic variant T/G snv 0.64 6
rs111305875 0.827 0.120 6 167098098 intron variant T/G snv 3.0E-02 5
rs12987977
IL18R1
0.827 0.120 2 102358876 intron variant T/G snv 0.31 5
rs6425143 0.827 0.120 1 172875212 intron variant T/G snv 0.34 5
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 5
rs7765379 0.827 0.280 6 32713151 upstream gene variant T/G snv 0.10 3
rs10185424 0.925 0.040 2 102046427 intron variant T/G snv 0.62 2
rs1819333 1.000 0.040 6 166960059 upstream gene variant T/G snv 0.57 2
rs2315008
ZGPAT
0.925 0.120 20 63712604 intron variant T/G snv 0.70 2
rs1063355
HLA-DQB1-AS1 ; HLA-DQB1
0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56 1
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 1
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
rs17582416 0.882 0.160 10 34998722 regulatory region variant T/G snv 0.31 1
rs17695092
CPEB4
1.000 0.040 5 173910850 intron variant T/G snv 0.22 1
rs72981516
FCHSD2
1.000 0.040 11 72959855 intron variant T/G snv 6.2E-05 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs4921482
LOC285626
0.807 0.120 5 159337470 intron variant T/C;G snv 6
rs7097656
TSPAN14
0.827 0.120 10 80491075 intron variant T/C;G snv 6