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
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 3
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
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
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
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
rs6908425
CDKAL1
0.752 0.320 6 20728500 intron variant T/C snv 0.78 3
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 3
rs762421
GATD3A
0.851 0.360 21 44195678 intron variant G/A snv 3
rs8005161
GPR65
0.882 0.120 14 88006251 intron variant C/T snv 0.18 3
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 4
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs11167764
LOC105378204
0.925 0.120 5 142099500 regulatory region variant A/C snv 0.80 2
rs17582416 0.882 0.160 10 34998722 regulatory region variant T/G snv 0.31 3
rs4613763 0.851 0.240 5 40392626 regulatory region variant T/C snv 0.14 3
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 3
rs199883290
NOD2
0.925 0.120 16 50729867 missense variant G/A;C snv 4.0E-06; 1.5E-02 7.0E-06 2