rs174570, FADS2

N. diseases: 11
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
1243 0.882 0.200 11 61829740 intron variant C/T snv 0.15 0.800 1.000 3 2009 2019
Low density lipoprotein cholesterol measurement
1142 0.882 0.200 11 61829740 intron variant C/T snv 0.15 0.800 1.000 2 2009 2019
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.882 0.200 11 61829740 intron variant C/T snv 0.15 0.700 1.000 2 2012 2013
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.882 0.200 11 61829740 intron variant C/T snv 0.15 0.800 1.000 2 2012 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.882 0.200 11 61829740 intron variant C/T snv 0.15 0.700 1.000 1 2011 2011
High density lipoprotein measurement
1440 0.882 0.200 11 61829740 intron variant C/T snv 0.15 0.700 1.000 1 2012 2012
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.882 0.200 11 61829740 intron variant C/T snv 0.15 0.700 1.000 1 2011 2011
Phospholipid measurement
CUI: C0202177
Disease: Phospholipid measurement
306 0.882 0.200 11 61829740 intron variant C/T snv 0.15 0.700 1.000 1 2011 2011
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
363 0.882 0.200 11 61829740 intron variant C/T snv 0.15 0.010 1.000 1 2016 2016
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.882 0.200 11 61829740 intron variant C/T snv 0.15 0.700 1.000 1 2012 2012
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 0.882 0.200 11 61829740 intron variant C/T snv 0.15 0.700 1.000 1 2009 2009