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: rs1801253
rs1801253
0.707 0.214 10 114045297 missense variant G/C snp 0.74 0.70
CUI: C0005612
Disease: Birth Weight
Birth Weight
Pathological Conditions, Signs and Symptoms 0.800 1 2013 2013
dbSNP: rs1801253
rs1801253
0.707 0.214 10 114045297 missense variant G/C snp 0.74 0.70
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
Cardiovascular Diseases 0.080 1.000 8 2003 2013
dbSNP: rs1801253
rs1801253
0.707 0.214 10 114045297 missense variant G/C snp 0.74 0.70
CUI: C0018801
Disease: Heart failure
Heart failure
Cardiovascular Diseases 0.060 1.000 6 2003 2013
dbSNP: rs1801253
rs1801253
0.707 0.214 10 114045297 missense variant G/C snp 0.74 0.70
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.040 1.000 4 2001 2011
dbSNP: rs1801252
rs1801252
0.756 0.179 10 114044277 missense variant A/G snp 0.15 0.17
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
Cardiovascular Diseases 0.030 0.667 3 2001 2013
dbSNP: rs1801252
rs1801252
0.756 0.179 10 114044277 missense variant A/G snp 0.15 0.17
CUI: C0018801
Disease: Heart failure
Heart failure
Cardiovascular Diseases 0.030 0.667 3 2001 2013
dbSNP: rs1801253
rs1801253
0.707 0.214 10 114045297 missense variant G/C snp 0.74 0.70
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
Cardiovascular Diseases; Pathological Conditions, Signs and Symptoms 0.030 1.000 3 2012 2014
dbSNP: rs1801252
rs1801252
0.756 0.179 10 114044277 missense variant A/G snp 0.15 0.17
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.020 < 0.001 2 2002 2006
dbSNP: rs1801252
rs1801252
0.756 0.179 10 114044277 missense variant A/G snp 0.15 0.17
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.020 0.500 2 2001 2009
dbSNP: rs1801253
rs1801253
0.707 0.214 10 114045297 missense variant G/C snp 0.74 0.70
CUI: C0264716
Disease: Chronic heart failure
Chronic heart failure
0.020 1.000 2 2011 2013
dbSNP: rs1801253
rs1801253
0.707 0.214 10 114045297 missense variant G/C snp 0.74 0.70
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic
Cardiovascular Diseases 0.020 1.000 2 2003 2012
dbSNP: rs1801253
rs1801253
0.707 0.214 10 114045297 missense variant G/C snp 0.74 0.70
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction
0.020 1.000 2 2003 2010
dbSNP: rs1801253
rs1801253
0.707 0.214 10 114045297 missense variant G/C snp 0.74 0.70
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.020 0.500 2 2002 2006
dbSNP: rs1801253
rs1801253
0.707 0.214 10 114045297 missense variant G/C snp 0.74 0.70
CUI: C0028754
Disease: Obesity
Obesity
Nutritional and Metabolic Diseases; Pathological Conditions, Signs and Symptoms 0.020 1.000 2 2007 2007
dbSNP: rs1801252
rs1801252
0.756 0.179 10 114044277 missense variant A/G snp 0.15 0.17
CUI: C0264657
Disease: Renal sclerosis with hypertension
Renal sclerosis with hypertension
0.010 1.000 1 2010 2010
dbSNP: rs1801252
rs1801252
0.756 0.179 10 114044277 missense variant A/G snp 0.15 0.17
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome
Cardiovascular Diseases 0.010 1.000 1 2005 2005
dbSNP: rs1801252
rs1801252
0.756 0.179 10 114044277 missense variant A/G snp 0.15 0.17
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic
Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs1801252
rs1801252
0.756 0.179 10 114044277 missense variant A/G snp 0.15 0.17
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
Cardiovascular Diseases 0.010 1.000 1 2009 2009
dbSNP: rs1801252
rs1801252
0.756 0.179 10 114044277 missense variant A/G snp 0.15 0.17
CUI: C0424166
Disease: Social Anxiety
Social Anxiety
Behavior and Behavior Mechanisms 0.010 1.000 1 2004 2004
dbSNP: rs1801252
rs1801252
0.756 0.179 10 114044277 missense variant A/G snp 0.15 0.17
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
Cardiovascular Diseases; Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2012 2012
dbSNP: rs1801253
rs1801253
0.707 0.214 10 114045297 missense variant G/C snp 0.74 0.70
CUI: C0085612
Disease: Ventricular arrhythmia
Ventricular arrhythmia
0.010 1.000 1 2008 2008
dbSNP: rs1801253
rs1801253
0.707 0.214 10 114045297 missense variant G/C snp 0.74 0.70
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
Cardiovascular Diseases 0.010 1.000 1 2006 2006
dbSNP: rs1801253
rs1801253
0.707 0.214 10 114045297 missense variant G/C snp 0.74 0.70
CUI: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy
Cardiovascular Diseases; Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2010 2010
dbSNP: rs1801253
rs1801253
0.707 0.214 10 114045297 missense variant G/C snp 0.74 0.70
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome
Cardiovascular Diseases 0.010 1.000 1 2005 2005
dbSNP: rs1801253
rs1801253
0.707 0.214 10 114045297 missense variant G/C snp 0.74 0.70
CUI: C0424166
Disease: Social Anxiety
Social Anxiety
Behavior and Behavior Mechanisms 0.010 1.000 1 2004 2004