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.
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
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
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
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
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
Gerstmann-Straussler-Scheinker Disease
39 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2016 2016
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
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
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
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 0.010 1.000 1 2017 2017
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