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.
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
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
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
1451 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
502 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2013 2013
Massive Osteolyses
CUI: C0029438
Disease: Massive Osteolyses
11 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2016 2016
Metabolic Diseases
CUI: C0025517
Disease: Metabolic Diseases
50 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2018 2018
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2009 2009
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2010 2010
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
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