EPHB2, EPH receptor B2, 2048

N. diseases: 649; N. variants: 19
Disease: Carcinogenesis ×
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: rs1018379423
rs1018379423 		1 22907986 missense variant G/T snv 4.0E-06 2.1E-05
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs746830376
rs746830376 		0.925 0.200 1 22784501 missense variant G/A snv 2.4E-05 3.5E-05
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2015 2015