CTSG, cathepsin G, 1511

N. diseases: 95; N. variants: 5
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: rs45567233
rs45567233 		0.882 0.200 14 24574465 missense variant T/C snv 8.0E-02 5.9E-02
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2001 2001