Disease: Crohn Disease
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs540973741
NOD2
0.925 0.120 16 50729868 frameshift variant C/-;CC delins 2
rs5743293
NOD2
0.807 0.200 16 50729868 frameshift variant C/-;CC delins 2
rs762421
GATD3A
0.851 0.360 21 44195678 intron variant G/A snv 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
rs2066847
NOD2
0.716 0.400 16 50729868 frameshift variant C/-;CC delins 1.5E-02 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
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 3
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs4613763 0.851 0.240 5 40392626 regulatory region variant T/C snv 0.14 3
rs8005161
GPR65
0.882 0.120 14 88006251 intron variant C/T snv 0.18 3
rs11747270
IRGM
0.790 0.240 5 150879305 intron variant A/G snv 0.21 3
rs11584383
MROH3P
0.827 0.200 1 200966738 downstream gene variant T/C snv 0.24 4
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 3
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 6
rs3764147
LACC1
0.807 0.280 13 43883789 missense variant A/G snv 0.28 0.27 4
rs2188962
IRF1-AS1
0.882 0.160 5 132435113 intron variant C/T snv 0.29 4
rs17582416 0.882 0.160 10 34998722 regulatory region variant T/G snv 0.31 3
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 3
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 4
rs1736135
LOC101927745
0.851 0.160 21 15432901 intron variant T/C snv 0.33 4
rs224136 0.925 0.120 10 62710915 intron variant C/A;T snv 0.34 2
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 5