REN, renin, 5972

N. diseases: 721; N. variants: 25
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: rs11571111
rs11571111 		1 204161105 intron variant C/A snv 5.0E-03
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11571111
rs11571111 		1 204161105 intron variant C/A snv 5.0E-03
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11571111
rs11571111 		1 204161105 intron variant C/A snv 5.0E-03
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11571111
rs11571111 		1 204161105 intron variant C/A snv 5.0E-03
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs193280350
rs193280350 		1 204179521 intron variant G/A snv 7.6E-03
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs6668858
rs6668858 		1 204166660 intron variant G/A snv 9.7E-03
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs6668858
rs6668858 		1 204166660 intron variant G/A snv 9.7E-03
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs6668858
rs6668858 		1 204166660 intron variant G/A snv 9.7E-03
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs6668858
rs6668858 		1 204166660 intron variant G/A snv 9.7E-03
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs6693954
rs6693954 		1 204163510 intron variant T/A snv 0.32
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs72749713
rs72749713 		1 204176450 intron variant G/A snv 2.6E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs5705
rs5705 		0.882 0.040 1 204162058 synonymous variant T/G snv 0.14 0.18
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs5705
rs5705 		0.882 0.040 1 204162058 synonymous variant T/G snv 0.14 0.18
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs5705
rs5705 		0.882 0.040 1 204162058 synonymous variant T/G snv 0.14 0.18
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs144219651
rs144219651 		0.925 0.080 1 204162017 missense variant A/T snv 8.0E-06 2.1E-05
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2011 2011
dbSNP: rs144219651
rs144219651 		0.925 0.080 1 204162017 missense variant A/T snv 8.0E-06 2.1E-05
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2011 2011
dbSNP: rs371237692
rs371237692 		0.925 0.120 1 204159515 synonymous variant A/G snv 8.0E-06 3.5E-05
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2008 2008
dbSNP: rs371237692
rs371237692 		0.925 0.120 1 204159515 synonymous variant A/G snv 8.0E-06 3.5E-05
CUI: C0577631
Disease: Carotid Atherosclerosis
Carotid Atherosclerosis 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2007 2007
dbSNP: rs371237692
rs371237692 		0.925 0.120 1 204159515 synonymous variant A/G snv 8.0E-06 3.5E-05
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2008 2008
dbSNP: rs371237692
rs371237692 		0.925 0.120 1 204159515 synonymous variant A/G snv 8.0E-06 3.5E-05
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2012 2012
dbSNP: rs371237692
rs371237692 		0.925 0.120 1 204159515 synonymous variant A/G snv 8.0E-06 3.5E-05
CUI: C0007820
Disease: Cerebrovascular Disorders
Cerebrovascular Disorders 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2007 2007
dbSNP: rs758564400
rs758564400 		0.925 0.120 1 204156683 missense variant A/G snv 4.0E-06
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic 		Digestive System Diseases; Infections 0.010 1.000 1 2009 2009
dbSNP: rs758564400
rs758564400 		0.925 0.120 1 204156683 missense variant A/G snv 4.0E-06
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs758564400
rs758564400 		0.925 0.120 1 204156683 missense variant A/G snv 4.0E-06
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2014 2014
dbSNP: rs758564400
rs758564400 		0.925 0.120 1 204156683 missense variant A/G snv 4.0E-06
CUI: C0023895
Disease: Liver diseases
Liver diseases 		Digestive System Diseases 0.010 1.000 1 2009 2009