IRGM, immunity related GTPase M, 345611

N. diseases: 6; N. variants: 5
Disease: Crohn Disease ×
Source: GWASCAT ×
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1000113
rs1000113 		0.925 0.040 5 150860514 intron variant C/T snv 0.13
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.840 1.000 1 2007 2015
dbSNP: rs11747270
rs11747270 		0.790 0.240 5 150879305 intron variant A/G snv 0.21
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.820 0.667 1 2008 2020
dbSNP: rs7714584
rs7714584 		1.000 0.040 5 150890858 intron variant A/G snv 0.21
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.800 1.000 1 2010 2010
dbSNP: rs11741861
rs11741861 		0.925 0.040 5 150898347 intron variant A/G snv 8.8E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 2 2015 2017
dbSNP: rs11749391
rs11749391 		0.827 0.120 5 150849504 intron variant T/C snv 0.21
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2016 2016