rs1137101, LEPR

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.
Amebic colitis
CUI: C0013370
Disease: Amebic colitis
1 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2014 2014
Hypertensive left ventricular hypertrophy
CUI: C1997092
Disease: Hypertensive left ventricular hypertrophy
1 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2013 2013
Liver Abscess, Amebic
CUI: C0023886
Disease: Liver Abscess, Amebic
1 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2014 2014
Non-ST-segment elevation myocardial infarction (NSTEMI)
CUI: C4700045
Disease: Non-ST-segment elevation myocardial infarction (NSTEMI)
1 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2018 2018
Amebiasis
CUI: C0002438
Disease: Amebiasis
2 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2014 2014
Non-ST Elevated Myocardial Infarction
CUI: C4255010
Disease: Non-ST Elevated Myocardial Infarction
2 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2018 2018
Obstructive sleep apnea hypopnea syndrome
CUI: C4285910
Disease: Obstructive sleep apnea hypopnea syndrome
7 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2019 2019
Gynecomastia
CUI: C0018418
Disease: Gynecomastia
8 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2014 2014
SHORT STATURE, IDIOPATHIC, X-LINKED
CUI: C1845118
Disease: SHORT STATURE, IDIOPATHIC, X-LINKED
8 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2012 2012
Nuchal bleb, familial
CUI: C0948242
Disease: Nuchal bleb, familial
9 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2006 2006
Post transplant diabetes mellitus
CUI: C1504532
Disease: Post transplant diabetes mellitus
11 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2019 2019
Hunger
CUI: C0020175
Disease: Hunger
12 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2009 2009
Somatotropin deficiency
CUI: C0271561
Disease: Somatotropin deficiency
14 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.020 1.000 2 2012 2016
Malignant neoplasm of oropharynx
CUI: C0153382
Disease: Malignant neoplasm of oropharynx
15 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2015 2015
Oropharyngeal Carcinoma
CUI: C2349952
Disease: Oropharyngeal Carcinoma
15 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2015 2015
Premenopausal breast cancer
CUI: C0741682
Disease: Premenopausal breast cancer
18 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2008 2008
Hyperlipidemia, Familial Combined
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
28 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2006 2006
Overweight and obesity
CUI: C1561826
Disease: Overweight and obesity
29 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.020 1.000 2 2016 2018
Squamous cell carcinoma of oropharynx
CUI: C0280313
Disease: Squamous cell carcinoma of oropharynx
33 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2015 2015
Pregnancy associated hypertension
CUI: C0852036
Disease: Pregnancy associated hypertension
43 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2010 2010
Acute leukemia
CUI: C0085669
Disease: Acute leukemia
50 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2006 2006
Diarrhea
CUI: C0011991
Disease: Diarrhea
63 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2014 2014
Pediatric Obesity
CUI: C2362324
Disease: Pediatric Obesity
67 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.020 1.000 2 2018 2018
Left Ventricular Hypertrophy
CUI: C0149721
Disease: Left Ventricular Hypertrophy
67 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2013 2013
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
81 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.020 1.000 2 2001 2005