Disease: Crohn Disease
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 3
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 3
rs11167764
LOC105378204
0.925 0.120 5 142099500 regulatory region variant A/C snv 0.80 2
rs11175593
LRRK2 ; LRRK2-DT ; LINC02471 ; LOC105369735
0.882 0.160 12 40208138 non coding transcript exon variant C/T snv 2.8E-02 3
rs11190140
NKX2-3 ; LINC01475
0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55 4
rs11584383
MROH3P
0.827 0.200 1 200966738 downstream gene variant T/C snv 0.24 4
rs11747270
IRGM
0.790 0.240 5 150879305 intron variant A/G snv 0.21 3
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs1456893 0.851 0.160 7 50230076 intron variant G/A snv 0.69 3
rs1551398
LOC105375746
0.882 0.160 8 125527809 intron variant G/A snv 0.48 3
rs1736135
LOC101927745
0.851 0.160 21 15432901 intron variant T/C snv 0.33 4
rs17582416 0.882 0.160 10 34998722 regulatory region variant T/G snv 0.31 3
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 3
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs2066847
NOD2
0.716 0.400 16 50729868 frameshift variant C/-;CC delins 1.5E-02 2
rs2188962
IRF1-AS1
0.882 0.160 5 132435113 intron variant C/T snv 0.29 4
rs224136 0.925 0.120 10 62710915 intron variant C/A;T snv 0.34 2
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 4
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs3828309
ATG16L1
0.882 0.160 2 233271764 intron variant A/G snv 0.42 3
rs4263839
TNFSF15
0.807 0.160 9 114804160 intron variant A/G snv 0.75 3
rs4613763 0.851 0.240 5 40392626 regulatory region variant T/C snv 0.14 3
rs540973741
NOD2
0.925 0.120 16 50729868 frameshift variant C/-;CC delins 2