rs56149945, NR3C1

N. diseases: 49
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.
Obesity
CUI: C0028754
Disease: Obesity
1111 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.070 0.714 7 2001 2010
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.050 1.000 5 2005 2016
Cushing Syndrome
CUI: C0010481
Disease: Cushing Syndrome
9 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.040 1.000 4 2012 2020
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.040 0.750 4 2003 2015
Adrenal Cushing's syndrome
CUI: C0342443
Disease: Adrenal Cushing's syndrome
9 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.030 1.000 3 2012 2020
Asthma
CUI: C0004096
Disease: Asthma
1536 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.030 1.000 3 2012 2016
Childhood Acute Lymphoblastic Leukemia
261 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.030 0.667 3 2005 2013
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.030 0.667 3 2001 2013
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.030 0.667 3 2003 2016
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.030 1.000 3 2007 2020
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.020 1.000 2 2006 2016
Chronic active hepatitis
CUI: C0520463
Disease: Chronic active hepatitis
34 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.020 1.000 2 2006 2009
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.020 0.500 2 2001 2003
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.020 0.500 2 2001 2003
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.020 0.500 2 2001 2013
Glucocorticoid Receptor Deficiency
CUI: C1841972
Disease: Glucocorticoid Receptor Deficiency
12 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.020 0.500 2 2006 2012
Pituitary-dependent Cushing's disease
8 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.020 0.500 2 2009 2014
social stress
CUI: C0871388
Disease: social stress
22 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.020 1.000 2 2004 2007
21-hydroxylase deficiency
CUI: C0852654
Disease: 21-hydroxylase deficiency
28 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.010 1.000 1 2006 2006
ACTH-Secreting Pituitary Adenoma
CUI: C1306214
Disease: ACTH-Secreting Pituitary Adenoma
5 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.010 1 2009 2009
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.010 1 2009 2009
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.010 1.000 1 2016 2016
Addison Disease
CUI: C0001403
Disease: Addison Disease
13 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.010 1.000 1 2012 2012
Adrenal incidentaloma
CUI: C2609247
Disease: Adrenal incidentaloma
2 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.010 1.000 1 2013 2013
Autoimmune disease (systemic) NOS
CUI: C2895206
Disease: Autoimmune disease (systemic) NOS
3 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 0.010 1 2018 2018