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.
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
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
Muscular stiffness
CUI: C0221170
Disease: Muscular stiffness
6 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2019 2019
Miscarriage
CUI: C4552766
Disease: Miscarriage
56 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2020 2020
Migraine with Aura
CUI: C0154723
Disease: Migraine with Aura
56 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2012 2012
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
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
Mental Depression
CUI: C0011570
Disease: Mental Depression
271 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2011 2011
Meniere Disease
CUI: C0025281
Disease: Meniere Disease
36 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2013 2013
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2010 2010
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
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.050 0.800 5 2012 2017
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
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
Male infertility
CUI: C0021364
Disease: Male infertility
146 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2014 2014
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
1451 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2012 2012
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.030 1.000 3 2011 2017
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
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2019 2019
Idiopathic scoliosis
CUI: C0595995
Disease: Idiopathic scoliosis
17 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1 2013 2013
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
Hormone refractory prostate cancer
CUI: C1328504
Disease: Hormone refractory prostate cancer
29 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2011 2011
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2014 2014
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2014 2014
Gynecomastia
CUI: C0018418
Disease: Gynecomastia
8 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2014 2014