rs1799883, FABP2

N. diseases: 36
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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 1998 1998
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.100 0.850 20 1999 2017
Obesity
CUI: C0028754
Disease: Obesity
1111 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.100 0.846 13 1999 2015
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.050 0.800 5 1999 2015
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.030 1.000 3 1999 2010
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.030 1.000 3 1999 2010
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
81 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 1999 1999
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.020 0.500 2 2000 2014
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.020 1.000 2 2001 2017
Hyperinsulinism
CUI: C0020459
Disease: Hyperinsulinism
64 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1 2001 2001
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
83 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1 2001 2001
Obesity, Morbid
CUI: C0028756
Disease: Obesity, Morbid
49 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2001 2001
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.080 0.875 8 2002 2015
Hyperlipidemia, Familial Combined
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
28 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2002 2002
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.030 1.000 3 2004 2013
Familial hypercholesterolemia - heterozygous
CUI: C0342882
Disease: Familial hypercholesterolemia - heterozygous
34 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2004 2004
Insulin resistance syndrome
CUI: C3714619
Disease: Insulin resistance syndrome
15 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2005 2005
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
140 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2005 2005
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.030 1.000 3 2006 2016
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2007 2007
Carotid Stenosis
CUI: C0007282
Disease: Carotid Stenosis
19 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1 2007 2007
Cerebrovascular Disorders
CUI: C0007820
Disease: Cerebrovascular Disorders
56 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2007 2007
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.020 1.000 2 2008 2014
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.020 1.000 2 2008 2015
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2009 2009