rs445925, APOC1

N. diseases: 10
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.
Low density lipoprotein cholesterol measurement
1142 0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 0.800 1.000 3 2011 2017
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 0.800 1.000 1 2011 2011
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 0.700 1.000 1 2012 2012
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 0.700 1.000 1 2013 2013
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
35 0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 0.700 1.000 1 2013 2013
Pseudocholinesterase Measurement
CUI: C1168443
Disease: Pseudocholinesterase Measurement
568 0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 0.700 1.000 1 2010 2010
RDW - Red blood cell distribution width result
988 0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 0.700 1.000 1 2017 2017
Red cell distribution width determination
988 0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 0.700 1.000 1 2017 2017
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 0.700 1.000 1 2012 2012
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 0.700 1.000 1 2011 2011