Disease: Crohn Disease
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 11
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 10
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 10
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs61839660
IL2RA
0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 9
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 8
rs2066844
NOD2
0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 5
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 3
rs76181804 0.925 0.120 1 198632575 intergenic variant A/G snv 8.2E-02 2