MYRF, myelin regulatory factor, 745

N. diseases: 102; N. variants: 44
Disease: Crohn Disease ×
Source: ALL
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: rs174535
rs174535 		0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs174537
rs174537 		0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2015 2015