FABP2, fatty acid binding protein 2, 2169

N. diseases: 65; N. variants: 2
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1799883
rs1799883 		0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.100 0.850 20 1999 2017
dbSNP: rs1799883
rs1799883 		0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.100 0.846 13 1999 2015
dbSNP: rs1799883
rs1799883 		0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.080 0.875 8 2002 2015
dbSNP: rs1799883
rs1799883 		0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias 		Nutritional and Metabolic Diseases 0.050 0.800 5 1999 2015
dbSNP: rs1799883
rs1799883 		0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.030 1.000 3 2004 2013
dbSNP: rs1799883
rs1799883 		0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.030 1.000 3 1999 2010
dbSNP: rs1799883
rs1799883 		0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.030 1.000 3 1999 2010
dbSNP: rs1799883
rs1799883 		0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		Nutritional and Metabolic Diseases 0.030 1.000 3 2006 2016
dbSNP: rs1799883
rs1799883 		0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.020 1.000 2 2008 2014
dbSNP: rs1799883
rs1799883 		0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		Nervous System Diseases; Cardiovascular Diseases 0.020 0.500 2 2000 2014
dbSNP: rs1799883
rs1799883 		0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		Cardiovascular Diseases 0.020 1.000 2 2001 2017
dbSNP: rs1799883
rs1799883 		0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.020 1.000 2 2008 2015
dbSNP: rs11724758
rs11724758 		0.925 0.080 4 119318723 3 prime UTR variant G/A snv 0.47
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs11724758
rs11724758 		0.925 0.080 4 119318723 3 prime UTR variant G/A snv 0.47
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.010 1.000 1 2013 2013
dbSNP: rs1799883
rs1799883 		0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0007282
Disease: Carotid Stenosis
Carotid Stenosis 		Nervous System Diseases; Cardiovascular Diseases 0.010 < 0.001 1 2007 2007
dbSNP: rs1799883
rs1799883 		0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.010 < 0.001 1 2013 2013
dbSNP: rs1799883
rs1799883 		0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0029438
Disease: Massive Osteolyses
Massive Osteolyses 		Musculoskeletal Diseases 0.010 1.000 1 2016 2016
dbSNP: rs1799883
rs1799883 		0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
Hyperlipidemia, Familial Combined 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.010 1.000 1 2002 2002
dbSNP: rs1799883
rs1799883 		0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance 		Nutritional and Metabolic Diseases 0.010 1.000 1 1999 1999
dbSNP: rs1799883
rs1799883 		0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism 		Nutritional and Metabolic Diseases 0.010 < 0.001 1 2001 2001
dbSNP: rs1799883
rs1799883 		0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C3714619
Disease: Insulin resistance syndrome
Insulin resistance syndrome 		Nutritional and Metabolic Diseases 0.010 1.000 1 2005 2005
dbSNP: rs1799883
rs1799883 		0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1799883
rs1799883 		0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2005 2005
dbSNP: rs1799883
rs1799883 		0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0007820
Disease: Cerebrovascular Disorders
Cerebrovascular Disorders 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2007 2007
dbSNP: rs1799883
rs1799883 		0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0028756
Disease: Obesity, Morbid
Obesity, Morbid 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2001 2001