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.
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
Asthma
CUI: C0004096
Disease: Asthma
1536 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2009 2009
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
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
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
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
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 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
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
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
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
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.020 0.500 2 2003 2014
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.020 0.500 2 2003 2014
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2014 2014
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
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
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
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
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2014 2014
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2014 2014
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 0.010 1.000 1 2014 2014
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
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
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