rs3764261, None

N. diseases: 11
Source: BEFREE ×
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.
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
390 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 0.860 1.000 6 2010 2018
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
477 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 0.830 1.000 3 2010 2018
Polypoidal choroidal vasculopathy
CUI: C1504336
Disease: Polypoidal choroidal vasculopathy
67 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 0.040 1.000 4 2013 2018
Aortic Aneurysm, Abdominal
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
78 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 0.010 1.000 1 2018 2018
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
382 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 0.010 1 2015 2015
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
1598 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 0.010 1 2015 2015
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 0.010 1.000 1 2015 2015
Glycogen storage disease type II
CUI: C0017921
Disease: Glycogen storage disease type II
80 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 0.010 1.000 1 2014 2014
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
871 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 0.010 1.000 1 2017 2017
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
547 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 0.010 1.000 1 2014 2014
Obesity
CUI: C0028754
Disease: Obesity
900 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 0.010 1.000 1 2015 2015