rs2234693, ESR1

N. diseases: 77
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.
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.030 0.667 3 2005 2013
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.020 1.000 2 2005 2019
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.020 1.000 2 2005 2009
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.100 1.000 11 2007 2020
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.100 1.000 10 2007 2020
Ventricular Fibrillation, Paroxysmal Familial, 1
CUI: C2751898
Disease: Ventricular Fibrillation, Paroxysmal Familial, 1
8 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2007 2007
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.040 1.000 4 2008 2014
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.020 1.000 2 2008 2009
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
197 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.020 1.000 2 2008 2009
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1 2008 2008
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.020 0.500 2 2009 2013
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.020 1.000 2 2009 2013
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.020 1.000 2 2009 2018
Obesity
CUI: C0028754
Disease: Obesity
1111 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2009 2009
Osteoarthritis of the hand
CUI: C0263746
Disease: Osteoarthritis of the hand
21 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1 2009 2009
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2009 2009
Shared Paranoid Disorder
CUI: C0036939
Disease: Shared Paranoid Disorder
10 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2009 2009
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.020 0.500 2 2010 2015
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
247 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.020 1.000 2 2010 2015
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.020 1.000 2 2010 2018
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.020 1.000 2 2010 2017
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.020 1.000 2 2010 2018
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2010 2010
Hypercholesterolemia
CUI: C0020443
Disease: Hypercholesterolemia
123 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2010 2010
leukemia
CUI: C0023418
Disease: leukemia
144 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2010 2010