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.
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
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2017 2017
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2015 2015
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
Sleep Apnea, Obstructive
CUI: C0520679
Disease: Sleep Apnea, Obstructive
105 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.060 1.000 6 2007 2019
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
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2010 2010
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2018 2018
Psychotic Disorders
CUI: C0033975
Disease: Psychotic Disorders
179 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.020 1.000 2 2011 2019
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.020 1.000 2 2003 2016
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2014 2014
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.040 0.250 4 2012 2019
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
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
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
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.040 0.750 4 2013 2019
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
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
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
182 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2013 2013
Osteoarthritis, Knee
CUI: C0409959
Disease: Osteoarthritis, Knee
150 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2016 2016
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
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
Obesity
CUI: C0028754
Disease: Obesity
1111 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.100 0.903 31 2001 2018
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
Nonorganic psychosis
CUI: C0349204
Disease: Nonorganic psychosis
98 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2019 2019