AGT, angiotensinogen, 183

N. diseases: 765; N. variants: 43
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: rs2004776
rs2004776 		1 230712956 intron variant C/G;T snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 4 2017 2018
dbSNP: rs2004776
rs2004776 		1 230712956 intron variant C/G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 2 2017 2018
dbSNP: rs2004776
rs2004776 		1 230712956 intron variant C/G;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.020 1.000 2 2011 2019
dbSNP: rs2493134
rs2493134 		1 230713613 intron variant T/C snv 0.57
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.020 1.000 2 2016 2019
dbSNP: rs1078499
rs1078499 		1 230713350 intron variant A/G snv 0.30
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs11568023
rs11568023 		1 230712433 intron variant G/A;T snv
CUI: C0018799
Disease: Heart Diseases
Heart Diseases 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs11568026
rs11568026 		1 230711777 intron variant A/G snv 3.7E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11568026
rs11568026 		1 230711777 intron variant A/G snv 3.7E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11568054
rs11568054 		1 230709809 intron variant G/A snv 3.6E-02
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2013 2013
dbSNP: rs2004776
rs2004776 		1 230712956 intron variant C/G;T snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs2004776
rs2004776 		1 230712956 intron variant C/G;T snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs2148582
rs2148582 		1 230714053 intron variant A/G snv 0.58
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs2148582
rs2148582 		1 230714053 intron variant A/G snv 0.58
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs2478539
rs2478539 		1 230709026 intron variant G/T snv 0.57
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs2478543
rs2478543 		1 230708564 intron variant T/C snv 0.58
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs2493132
rs2493132 		1 230707811 intron variant T/C;G snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs2493134
rs2493134 		1 230713613 intron variant T/C snv 0.57
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2016 2016
dbSNP: rs2493134
rs2493134 		1 230713613 intron variant T/C snv 0.57
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2016 2016
dbSNP: rs2493134
rs2493134 		1 230713613 intron variant T/C snv 0.57
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs3789671
rs3789671 		1 230708054 intron variant G/A;T snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs6687360
rs6687360 		1 230709246 intron variant C/T snv 0.45
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs7079
rs7079 		1 230702585 3 prime UTR variant G/T snv 0.25
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs699
rs699 		0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.100 0.865 89 1994 2019
dbSNP: rs699
rs699 		0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		Cardiovascular Diseases 0.100 0.795 39 1993 2014
dbSNP: rs699
rs699 		0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases 0.100 0.905 21 1996 2018