rs174570, FADS2

N. diseases: 9
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 total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
814 0.878 0.179 11 61829740 intron variant C/T snp 0.16 0.800 2 2009 2012
Low density lipoprotein cholesterol measurement
676 0.878 0.179 11 61829740 intron variant C/T snp 0.16 0.800 1 2009 2009
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
3393 0.878 0.179 11 61829740 intron variant C/T snp 0.16 0.700 2 2012 2013
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
735 0.878 0.179 11 61829740 intron variant C/T snp 0.16 0.700 1 2011 2011
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
760 0.878 0.179 11 61829740 intron variant C/T snp 0.16 0.700 1 2011 2011
High density lipoprotein measurement
867 0.878 0.179 11 61829740 intron variant C/T snp 0.16 0.700 1 2012 2012
Phospholipid measurement
CUI: C0202177
Disease: Phospholipid measurement
301 0.878 0.179 11 61829740 intron variant C/T snp 0.16 0.700 1 2011 2011
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
923 0.878 0.179 11 61829740 intron variant C/T snp 0.16 0.700 1 2012 2012
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
181 0.878 0.179 11 61829740 intron variant C/T snp 0.16 0.010 1.000 1 2016 2016