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.
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
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