rs12721046, APOC1

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.
High density lipoprotein measurement
1440 19 44917997 intron variant G/A snv 0.11 0.700 1.000 2 2012 2012
Low density lipoprotein cholesterol measurement
1142 19 44917997 intron variant G/A snv 0.11 0.700 1.000 2 2012 2012
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 19 44917997 intron variant G/A snv 0.11 0.700 1.000 2 2012 2012
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 19 44917997 intron variant G/A snv 0.11 0.700 1.000 2 2012 2012
C-reactive protein measurement
CUI: C0201657
Disease: C-reactive protein measurement
624 19 44917997 intron variant G/A snv 0.11 0.700 1.000 1 2013 2013
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 19 44917997 intron variant G/A snv 0.11 0.700 1.000 1 2012 2012
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 19 44917997 intron variant G/A snv 0.11 0.700 1.000 1 2012 2012
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 19 44917997 intron variant G/A snv 0.11 0.700 1.000 1 2012 2012