rs662799, APOA5

N. diseases: 33
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.
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1.000 1 2014 2014
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1.000 1 2014 2014
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1.000 1 2017 2017
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
83 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1.000 1 2018 2018
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1.000 1 2018 2018
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1.000 1 2011 2011
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1 2018 2018
Nuchal bleb, familial
CUI: C0948242
Disease: Nuchal bleb, familial
9 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.010 1.000 1 2010 2010