rs174555, FADS2;FADS1

N. diseases: 4
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 11 61812288 intron variant T/C snv 0.26 0.700 1.000 2 2012 2013
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 11 61812288 intron variant T/C snv 0.26 0.700 1.000 1 2016 2016
Granulocyte count
CUI: C0857490
Disease: Granulocyte count
150 11 61812288 intron variant T/C snv 0.26 0.700 1.000 1 2016 2016
Neutrophil count (procedure)
CUI: C0200633
Disease: Neutrophil count (procedure)
234 11 61812288 intron variant T/C snv 0.26 0.700 1.000 1 2016 2016