rs6589566, ZPR1

N. diseases: 8
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.
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
923 1.000 0.036 11 116781707 intron variant G/A,C,T snp 0.93 0.800 2 2012 2013
Low density lipoprotein cholesterol measurement
676 1.000 0.036 11 116781707 intron variant G/A,C,T snp 0.93 0.800 1 2008 2008
Aspartate aminotransferase measurement
108 1.000 0.036 11 116781707 intron variant G/A,C,T snp 0.93 0.700 1 2011 2011
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
3393 1.000 0.036 11 116781707 intron variant G/A,C,T snp 0.93 0.700 1 2012 2012
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
760 1.000 0.036 11 116781707 intron variant G/A,C,T snp 0.93 0.700 1 2011 2011
Ferritin measurement
CUI: C0373607
Disease: Ferritin measurement
155 1.000 0.036 11 116781707 intron variant G/A,C,T snp 0.93 0.700 1 2011 2011
response to statin
CUI: C3549252
Disease: response to statin
166 1.000 0.036 11 116781707 intron variant G/A,C,T snp 0.93 0.700 1 2011 2011
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
814 1.000 0.036 11 116781707 intron variant G/A,C,T snp 0.93 0.700 1 2012 2012