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: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.100 0.850 20 1999 2017
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0028754
Disease: Obesity
Obesity 		0.100 0.846 13 1999 2015
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.080 0.875 8 2002 2015
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias 		0.050 0.800 5 1999 2015
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.030 1.000 3 2006 2016
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.030 1.000 3 1999 2010
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0011847
Disease: Diabetes
Diabetes 		0.030 1.000 3 1999 2010
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.030 1.000 3 2004 2013
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
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.020 1.000 2 2008 2015
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.020 0.500 2 2000 2014
dbSNP: rs1799883
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.020 1.000 2 2001 2017
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