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: rs11053646
rs11053646
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.720 1.000 2 2003 2004
dbSNP: rs12316150
rs12316150
1.000 0.080 12 10159692 3 prime UTR variant A/T snv 7.4E-02
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 0
dbSNP: rs11053646
rs11053646
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.050 0.800 5 2003 2017
dbSNP: rs11053646
rs11053646
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.030 1.000 3 2003 2011
dbSNP: rs11053646
rs11053646
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
Cardiovascular Diseases 0.030 1.000 3 2003 2011
dbSNP: rs11053646
rs11053646
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
Nervous System Diseases; Cardiovascular Diseases 0.020 1.000 2 2006 2015
dbSNP: rs1050283
rs1050283
0.882 0.160 12 10159690 3 prime UTR variant G/A snv 0.40
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs1050283
rs1050283
0.882 0.160 12 10159690 3 prime UTR variant G/A snv 0.40
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction
0.010 1.000 1 2014 2014
dbSNP: rs1050283
rs1050283
0.882 0.160 12 10159690 3 prime UTR variant G/A snv 0.40
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs1050283
rs1050283
0.882 0.160 12 10159690 3 prime UTR variant G/A snv 0.40
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1050286
rs1050286
0.882 0.160 12 10158964 3 prime UTR variant T/C snv 0.40
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs1050286
rs1050286
0.882 0.160 12 10158964 3 prime UTR variant T/C snv 0.40
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs1050286
rs1050286
0.882 0.160 12 10158964 3 prime UTR variant T/C snv 0.40
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs11053646
rs11053646
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13
CUI: C0151744
Disease: Myocardial Ischemia
Myocardial Ischemia
Cardiovascular Diseases 0.010 1.000 1 2003 2003
dbSNP: rs11053646
rs11053646
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
Cardiovascular Diseases 0.010 1.000 1 2006 2006
dbSNP: rs11053646
rs11053646
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
Cardiovascular Diseases 0.010 1.000 1 2008 2008
dbSNP: rs11053646
rs11053646
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13
CUI: C0852949
Disease: Arteriopathic disease
Arteriopathic disease
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs11053646
rs11053646
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13
CUI: C0007820
Disease: Cerebrovascular Disorders
Cerebrovascular Disorders
Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2006 2006
dbSNP: rs11053646
rs11053646
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2010 2010
dbSNP: rs11053646
rs11053646
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13
CUI: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs11053646
rs11053646
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs11053646
rs11053646
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
Hyperlipoproteinemia Type IIa
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs11053646
rs11053646
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs11053646
rs11053646
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs11053646
rs11053646
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome
Cardiovascular Diseases 0.010 1.000 1 2010 2010