rs2144300, GALNT2

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.
High density lipoprotein measurement
1440 0.882 0.040 1 230159169 intron variant C/T snv 0.44 0.800 1.000 5 2008 2018
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.882 0.040 1 230159169 intron variant C/T snv 0.44 0.800 1.000 4 2008 2018
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.882 0.040 1 230159169 intron variant C/T snv 0.44 0.710 1.000 2 2011 2013
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.882 0.040 1 230159169 intron variant C/T snv 0.44 0.700 1.000 2 2008 2012
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.882 0.040 1 230159169 intron variant C/T snv 0.44 0.010 1.000 1 2013 2013
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.882 0.040 1 230159169 intron variant C/T snv 0.44 0.010 1.000 1 2013 2013
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.882 0.040 1 230159169 intron variant C/T snv 0.44 0.010 1.000 1 2013 2013