rs1799883, FABP2

N. diseases: 36
Source: BEFREE ×
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
769 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 1998 1998
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
80 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 1999 1999
Hyperinsulinism
CUI: C0020459
Disease: Hyperinsulinism
59 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
48 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2001 2001
Hyperlipidemia, Familial Combined
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
26 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2002 2002
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
131 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2005 2005
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
72 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
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
155 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2009 2009
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
547 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2009 2009
Diabetes
CUI: C0011847
Disease: Diabetes
611 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
714 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.030 1.000 3 1999 2010
hearing impairment
CUI: C1384666
Disease: hearing impairment
88 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2010 2010
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
189 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2010 2010
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
382 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.030 1.000 3 2004 2013
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1186 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2013 2013
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
362 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1 2013 2013
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2013 2013
Recurrent depression
CUI: C0221480
Disease: Recurrent depression
12 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2013 2013
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
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
412 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.020 0.500 2 2000 2014