Disease: Crohn Disease
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 3
rs8005161
GPR65
0.882 0.120 14 88006251 intron variant C/T snv 0.18 3
rs11167764
LOC105378204
0.925 0.120 5 142099500 regulatory region variant A/C snv 0.80 2
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
rs224136 0.925 0.120 10 62710915 intron variant C/A;T snv 0.34 2
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