rs174577, FADS2

N. diseases: 13
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.
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 1.000 0.080 11 61837342 intron variant C/A snv 0.38 0.800 1.000 2 2012 2018
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 1.000 0.080 11 61837342 intron variant C/A snv 0.38 0.800 1.000 2 2012 2018
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 1.000 0.080 11 61837342 intron variant C/A snv 0.38 0.700 1.000 2 2012 2013
Arachidonic acid measurement
CUI: C2316832
Disease: Arachidonic acid measurement
4 1.000 0.080 11 61837342 intron variant C/A snv 0.38 0.700 1.000 1 2015 2015
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 1.000 0.080 11 61837342 intron variant C/A snv 0.38 0.700 1.000 1 2018 2018
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 1.000 0.080 11 61837342 intron variant C/A snv 0.38 0.700 1.000 1 2011 2011
P wave duration (observable entity)
CUI: C0429021
Disease: P wave duration (observable entity)
18 1.000 0.080 11 61837342 intron variant C/A snv 0.38 0.700 1.000 1 2014 2014
QRS complex feature
CUI: C0429097
Disease: QRS complex feature
69 1.000 0.080 11 61837342 intron variant C/A snv 0.38 0.700 1.000 1 2016 2016
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 1.000 0.080 11 61837342 intron variant C/A snv 0.38 0.700 1.000 1 2012 2012
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 1.000 0.080 11 61837342 intron variant C/A snv 0.38 0.700 1.000 1 2018 2018
Serum transferrin measurement
CUI: C0428545
Disease: Serum transferrin measurement
10 1.000 0.080 11 61837342 intron variant C/A snv 0.38 0.700 1.000 1 2014 2014
Transferrin measurement
CUI: C0202105
Disease: Transferrin measurement
10 1.000 0.080 11 61837342 intron variant C/A snv 0.38 0.700 1.000 1 2014 2014
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 1.000 0.080 11 61837342 intron variant C/A snv 0.38 0.010 1.000 1 2016 2016