rs6065904, PLTP

N. diseases: 7
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.
Lipids measurement
CUI: C0523744
Disease: Lipids measurement
53 1.000 0.080 20 45906012 intron variant G/A snv 0.23 0.800 1.000 2 2009 2012
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 1.000 0.080 20 45906012 intron variant G/A snv 0.23 0.700 1.000 1 2018 2018
Gambling, Pathological
CUI: C0030662
Disease: Gambling, Pathological
9 1.000 0.080 20 45906012 intron variant G/A snv 0.23 0.700 1.000 1 2016 2016
High density lipoprotein measurement
1440 1.000 0.080 20 45906012 intron variant G/A snv 0.23 0.700 1.000 1 2012 2012
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 1.000 0.080 20 45906012 intron variant G/A snv 0.23 0.700 1.000 1 2012 2012
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 1.000 0.080 20 45906012 intron variant G/A snv 0.23 0.700 1.000 1 2012 2012
Carotid Artery Diseases
CUI: C0007273
Disease: Carotid Artery Diseases
6 1.000 0.080 20 45906012 intron variant G/A snv 0.23 0.010 1.000 1 2010 2010