Disease: Inflammatory Bowel Diseases
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 8
rs477515
HLA-DRB1
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 7
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 6
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs2188962
IRF1-AS1
0.882 0.160 5 132435113 intron variant C/T snv 0.29 4
rs1250550
ZMIZ1
0.851 0.240 10 79300560 intron variant C/A snv 0.27 3
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 3
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 3
rs2006996 0.882 0.080 9 114830358 regulatory region variant T/C snv 7.2E-02 3
rs7554511
INAVA
0.925 0.040 1 200908434 intron variant C/A snv 0.22 3
rs8005161
GPR65
0.882 0.120 14 88006251 intron variant C/T snv 0.18 3
rs10495903
THADA
1.000 0.040 2 43579779 intron variant C/T snv 0.13 2
rs10761659 0.925 0.040 10 62685804 intron variant A/G snv 0.43 2
rs11564258
MUC19 ; LOC105369736
1.000 0.040 12 40398498 intron variant G/A snv 3.1E-02 2
rs11742570 0.925 0.040 5 40410482 upstream gene variant T/C;G snv 2
rs1456896 0.882 0.200 7 50264865 upstream gene variant C/T snv 0.67 2
rs2076756
NOD2
0.882 0.040 16 50722970 intron variant A/G snv 0.17 2
rs2413583 0.925 0.040 22 39263768 intron variant C/T snv 0.19 2
rs3091316 1.000 0.040 17 34266955 upstream gene variant G/A;C snv 2
rs4409764 0.925 0.040 10 99524480 upstream gene variant T/A;G snv 2
rs5743289
NOD2
1.000 0.040 16 50722863 intron variant C/G;T snv 2
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 2