Disease: Crohn Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs3732378
CX3CR1
0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs696
NFKBIA
0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45 22
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 9
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8
rs11574938
ITGAL
0.827 0.120 16 30474072 missense variant G/A;C snv 0.62 6
rs1456896 0.882 0.200 7 50264865 upstream gene variant C/T snv 0.67 5
rs2631367
MIR3936HG ; SLC22A5
0.925 0.120 5 132369766 5 prime UTR variant C/G snv 0.59 4