FGFR1OP, FGFR1 oncogene partner, 11116

N. diseases: 40; N. variants: 9
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: rs2301436
rs2301436 		0.752 0.320 6 167024500 intron variant C/T snv 0.42
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.810 1.000 4 2008 2016
dbSNP: rs7749278
rs7749278 		1.000 0.040 6 167021837 intron variant T/C snv 0.43
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2008 2008