rs12149545, None

N. diseases: 7
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.
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.851 0.080 16 56959249 upstream gene variant G/A snv 0.23 0.700 1.000 1 2018 2018
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.851 0.080 16 56959249 upstream gene variant G/A snv 0.23 0.700 1.000 1 2012 2012
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.851 0.080 16 56959249 upstream gene variant G/A snv 0.23 0.010 1.000 1 2013 2013
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.851 0.080 16 56959249 upstream gene variant G/A snv 0.23 0.010 1.000 1 2015 2015
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.851 0.080 16 56959249 upstream gene variant G/A snv 0.23 0.010 1.000 1 2017 2017
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.851 0.080 16 56959249 upstream gene variant G/A snv 0.23 0.010 1.000 1 2017 2017
recurrent myocardial infarction
CUI: C4290140
Disease: recurrent myocardial infarction
6 0.851 0.080 16 56959249 upstream gene variant G/A snv 0.23 0.010 1.000 1 2013 2013