rs1137100, LEPR

N. diseases: 39
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.
HELLP Syndrome
CUI: C0162739
Disease: HELLP Syndrome
10 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2010 2010
Severe periodontitis
CUI: C4025886
Disease: Severe periodontitis
12 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2019 2019
Somatotropin deficiency
CUI: C0271561
Disease: Somatotropin deficiency
14 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2016 2016
Dystrophia myotonica 2
CUI: C2931689
Disease: Dystrophia myotonica 2
21 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2014 2014
Meningomyelocele
CUI: C0025312
Disease: Meningomyelocele
27 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2013 2013
Spina Bifida
CUI: C0080178
Disease: Spina Bifida
61 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2011 2011
Steatohepatitis
CUI: C2711227
Disease: Steatohepatitis
75 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2013 2013
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
81 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.020 1.000 2 2001 2005
Liver diseases
CUI: C0023895
Disease: Liver diseases
100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2013 2013
Lip and Oral Cavity Carcinoma
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
172 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1 2019 2019
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
182 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2013 2013
Malignant neoplasm of mouth
CUI: C0153381
Disease: Malignant neoplasm of mouth
184 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1 2019 2019
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.020 1.000 2 2013 2018
Conventional (Clear Cell) Renal Cell Carcinoma
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
222 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2014 2014
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1 2011 2011
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.020 1.000 2 2010 2015
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.020 1.000 2 2010 2015
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2014 2014
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2017 2017
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2015 2015
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2015 2015
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2014 2014
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2012 2012
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2012 2012
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2014 2014