Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		0.010 1.000 1 2010 2010
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2013 2013
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2013 2013
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance 		0.010 1.000 1 1999 1999
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0007820
Disease: Cerebrovascular Disorders
Cerebrovascular Disorders 		0.010 1.000 1 2007 2007
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		0.010 1.000 1 2009 2009
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.010 < 0.001 1 2013 2013
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia 		0.010 < 0.001 1 2001 2001
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0221480
Disease: Recurrent depression
Recurrent depression 		0.010 1.000 1 2013 2013
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 1998 1998
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0020474
Disease: Hyperlipidemia, Familial Combined
Hyperlipidemia, Familial Combined 		0.010 1.000 1 2002 2002
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases 		0.010 1.000 1 2005 2005
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0577631
Disease: Carotid Atherosclerosis
Carotid Atherosclerosis 		0.010 1.000 1 2007 2007
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0017495
Disease: Gerstmann-Straussler-Scheinker Disease
Gerstmann-Straussler-Scheinker Disease 		0.010 1.000 1 2016 2016
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C3714619
Disease: Insulin resistance syndrome
Insulin resistance syndrome 		0.010 1.000 1 2005 2005
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C1384666
Disease: hearing impairment
hearing impairment 		0.010 1.000 1 2010 2010
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0025517
Disease: Metabolic Diseases
Metabolic Diseases 		0.010 1.000 1 2018 2018
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0029438
Disease: Massive Osteolyses
Massive Osteolyses 		0.010 1.000 1 2016 2016
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.010 1.000 1 2017 2017
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0007282
Disease: Carotid Stenosis
Carotid Stenosis 		0.010 < 0.001 1 2007 2007
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0342882
Disease: Familial hypercholesterolemia - heterozygous
Familial hypercholesterolemia - heterozygous 		0.010 1.000 1 2004 2004
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism 		0.010 < 0.001 1 2001 2001
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0028756
Disease: Obesity, Morbid
Obesity, Morbid 		0.010 1.000 1 2001 2001
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 1.000 1 2009 2009
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction 		0.020 1.000 2 2008 2014