DDX39B, DExD-box helicase 39B, 7919

N. diseases: 50; N. variants: 23
Disease: Myocardial Infarction ×
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: rs2239527
rs2239527 		1.000 0.080 6 31542002 5 prime UTR variant C/G snv 0.33 0.38
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2007 2007