AGT, angiotensinogen, 183

N. diseases: 765; N. variants: 43
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: rs699
rs699 		0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.100 0.850 20 1995 2016
dbSNP: rs4762
rs4762 		0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.020 1.000 2 1999 2015
dbSNP: rs1177506410
rs1177506410 		0.776 0.240 1 230706148 missense variant G/C snv 4.0E-06 7.0E-06
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2001 2001
dbSNP: rs1275805226
rs1275805226 		0.776 0.240 1 230706148 frameshift variant G/- del 7.0E-06
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2001 2001
dbSNP: rs2067853
rs2067853 		0.851 0.160 1 230702512 downstream gene variant G/A snv 0.25
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs3789679
rs3789679 		0.925 0.120 1 230713948 intron variant G/A;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs5051
rs5051 		0.882 0.160 1 230714126 intron variant C/A;G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2013 2013