rs174556, FADS2;FADS1

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.
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.925 0.160 11 61813163 intron variant C/T snv 0.26 0.700 1.000 1 2008 2008
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.925 0.160 11 61813163 intron variant C/T snv 0.26 0.010 1.000 1 2011 2011
Phospholipid measurement
CUI: C0202177
Disease: Phospholipid measurement
306 0.925 0.160 11 61813163 intron variant C/T snv 0.26 0.700 1.000 1 2011 2011
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.925 0.160 11 61813163 intron variant C/T snv 0.26 0.700 1.000 2 2012 2013
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.925 0.160 11 61813163 intron variant C/T snv 0.26 0.010 1.000 1 2013 2013
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.925 0.160 11 61813163 intron variant C/T snv 0.26 0.010 1.000 1 2013 2013
Fatty acid measurement
CUI: C1281901
Disease: Fatty acid measurement
116 0.925 0.160 11 61813163 intron variant C/T snv 0.26 0.700 1.000 1 2018 2018