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
rs1456893 0.851 0.160 7 50230076 intron variant G/A snv 0.69 3
rs17582416 0.882 0.160 10 34998722 regulatory region variant T/G snv 0.31 3
rs224136 0.925 0.120 10 62710915 intron variant C/A;T snv 0.34 2
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
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
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 5
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 4
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs3828309
ATG16L1
0.882 0.160 2 233271764 intron variant A/G snv 0.42 3
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 3
rs6908425
CDKAL1
0.752 0.320 6 20728500 intron variant T/C snv 0.78 3
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 4
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
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 3
rs2188962
IRF1-AS1
0.882 0.160 5 132435113 intron variant C/T snv 0.29 4
rs11747270
IRGM
0.790 0.240 5 150879305 intron variant A/G snv 0.21 3
rs2274910
ITLN1
0.827 0.200 1 160882256 non coding transcript exon variant T/C snv 0.65 0.58 3
rs3764147
LACC1
0.807 0.280 13 43883789 missense variant A/G snv 0.28 0.27 4
rs1736135
LOC101927745
0.851 0.160 21 15432901 intron variant T/C snv 0.33 4