rs2067853, AGT

N. diseases: 5
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.851 0.160 1 230702512 downstream gene variant G/A snv 0.25 0.010 1.000 1 2013 2013
Hypoxic-Ischemic Encephalopathy
CUI: C0752304
Disease: Hypoxic-Ischemic Encephalopathy
12 0.851 0.160 1 230702512 downstream gene variant G/A snv 0.25 0.010 1.000 1 2019 2019
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.851 0.160 1 230702512 downstream gene variant G/A snv 0.25 0.010 1.000 1 2013 2013
Neonatal Hypoxic Ischemic Encephalopathy
CUI: C3898147
Disease: Neonatal Hypoxic Ischemic Encephalopathy
2 0.851 0.160 1 230702512 downstream gene variant G/A snv 0.25 0.010 1.000 1 2019 2019
Obesity
CUI: C0028754
Disease: Obesity
1111 0.851 0.160 1 230702512 downstream gene variant G/A snv 0.25 0.010 1.000 1 2013 2013