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.
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
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
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
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
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2008 2008
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
Asthma
CUI: C0004096
Disease: Asthma
1536 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2009 2009
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2009 2009
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2009 2009
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
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
103 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2009 2009
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1 2010 2010
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2010 2010
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2010 2010
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2010 2010
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
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
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.020 0.500 2 2004 2011
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2012 2012
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2012 2012
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
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
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
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
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