rs696217, GHRL;GHRLOS

N. diseases: 32
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.
METABOLIC SYNDROME, SUSCEPTIBILITY TO
CUI: C2676079
Disease: METABOLIC SYNDROME, SUSCEPTIBILITY TO
2 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.700 0
OBESITY, AGE AT ONSET OF
CUI: C4016925
Disease: OBESITY, AGE AT ONSET OF
1 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.700 0
Adenocarcinoma Of Esophagus
CUI: C0279628
Disease: Adenocarcinoma Of Esophagus
81 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2011 2011
Alcohol Use Disorder
CUI: C0001956
Disease: Alcohol Use Disorder
54 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2017 2017
Anorexia Nervosa
CUI: C0003125
Disease: Anorexia Nervosa
72 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2007 2007
Asthma
CUI: C0004096
Disease: Asthma
1536 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2009 2009
Bulimia Nervosa
CUI: C2267227
Disease: Bulimia Nervosa
24 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2006 2006
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1 2003 2003
Complications of Diabetes Mellitus
CUI: C0342257
Disease: Complications of Diabetes Mellitus
35 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2003 2003
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2008 2008
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2008 2008
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2008 2008
Depressed mood
CUI: C0344315
Disease: Depressed mood
269 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2017 2017
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
297 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2017 2017
Familial multiple trichoepitheliomata
CUI: C1275122
Disease: Familial multiple trichoepitheliomata
32 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2008 2008
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2015 2015
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2015 2015
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2014 2014
Mental Depression
CUI: C0011570
Disease: Mental Depression
271 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2017 2017
Overweight and obesity
CUI: C1561826
Disease: Overweight and obesity
29 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2019 2019
Pediatric Obesity
CUI: C2362324
Disease: Pediatric Obesity
67 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1 2005 2005
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2009 2009
Post-Traumatic Stress Disorder
CUI: C0038436
Disease: Post-Traumatic Stress Disorder
117 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2019 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2014 2014
Renal Insufficiency
CUI: C1565489
Disease: Renal Insufficiency
42 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2006 2006