rs1000778, FADS3

N. diseases: 3
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.
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 1.000 0.040 11 61887833 intron variant A/G snv 0.59 0.700 1.000 1 2012 2012
Phospholipid measurement
CUI: C0202177
Disease: Phospholipid measurement
306 1.000 0.040 11 61887833 intron variant A/G snv 0.59 0.700 1.000 1 2011 2011
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 1.000 0.040 11 61887833 intron variant A/G snv 0.59 0.010 1.000 1 2017 2017