Disease: Inflammatory Bowel Diseases
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 12
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 11
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 11
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 7
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 7
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 7
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 5
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 4