rs4846914, GALNT2

N. diseases: 6
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.
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.925 0.080 1 230159944 intron variant G/A snv 0.45 0.010 1.000 1 2010 2010
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.925 0.080 1 230159944 intron variant G/A snv 0.45 0.010 1.000 1 2010 2010
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.925 0.080 1 230159944 intron variant G/A snv 0.45 0.700 1.000 1 2011 2011
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.925 0.080 1 230159944 intron variant G/A snv 0.45 0.700 1.000 5 2008 2013
High density lipoprotein measurement
1440 0.925 0.080 1 230159944 intron variant G/A snv 0.45 0.800 1.000 9 2008 2019
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.925 0.080 1 230159944 intron variant G/A snv 0.45 0.800 1.000 7 2008 2019