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.
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
Unipolar Depression
CUI: C0041696
Disease: Unipolar Depression
225 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2012 2012
Turner Syndrome
CUI: C0041408
Disease: Turner Syndrome
21 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2019 2019
Tension Headache
CUI: C0033893
Disease: Tension Headache
6 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2010 2010
Takotsubo Cardiomyopathy
CUI: C1739395
Disease: Takotsubo Cardiomyopathy
3 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2017 2017
Sudden sensorineural hearing loss
CUI: C4275242
Disease: Sudden sensorineural hearing loss
38 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2013 2013
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
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
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.050 0.800 5 2012 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
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2015 2015
Premature Menopause
CUI: C0025322
Disease: Premature Menopause
90 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.020 1.000 2 2014 2015
Post-Traumatic Stress Disorder
CUI: C0038436
Disease: Post-Traumatic Stress Disorder
117 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2019 2019
Phobic anxiety disorder
CUI: C0349231
Disease: Phobic anxiety disorder
7 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2011 2011
Pelvic Organ Prolapse
CUI: C0877015
Disease: Pelvic Organ Prolapse
49 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2020 2020
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2014 2014
Ovarian Failure, Premature
CUI: C0085215
Disease: Ovarian Failure, Premature
115 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.020 1.000 2 2014 2015
Osteoporotic Fractures
CUI: C0521170
Disease: Osteoporotic Fractures
40 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2012 2012
Osteoporosis, Postmenopausal
CUI: C0029458
Disease: Osteoporosis, Postmenopausal
38 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2016 2016
Osteoarthritis, Knee
CUI: C0409959
Disease: Osteoarthritis, Knee
150 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2015 2015
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
Osteoarthritis of hip
CUI: C0029410
Disease: Osteoarthritis of hip
121 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2010 2010
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
Nephritis
CUI: C0027697
Disease: Nephritis
40 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1 2017 2017
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.555 0.680 6 151842200 intron variant T/C snv 0.47 0.010 1.000 1 2010 2010