AHSG, alpha 2-HS glycoprotein, 197

N. diseases: 204; N. variants: 18
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: rs4917
rs4917 		0.790 0.160 3 186619924 missense variant T/C snv 0.68 0.68
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.020 1.000 2 2009 2015
dbSNP: rs4918
rs4918 		0.763 0.400 3 186620593 missense variant G/A;C snv 0.67
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs761660984
rs761660984 		1.000 0.080 3 186620589 missense variant G/A;C;T snv 2.9E-05
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2015 2015