rs673548, APOB

N. diseases: 14
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
1418 0.925 0.120 2 21014672 intron variant G/A;T snv 0.800 1.000 5 2009 2019
High density lipoprotein measurement
1440 0.925 0.120 2 21014672 intron variant G/A;T snv 0.800 1.000 4 2012 2019
Low density lipoprotein cholesterol measurement
1142 0.925 0.120 2 21014672 intron variant G/A;T snv 0.800 1.000 2 2012 2018
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.925 0.120 2 21014672 intron variant G/A;T snv 0.800 1.000 2 2012 2018
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.925 0.120 2 21014672 intron variant G/A;T snv 0.800 1.000 1 2012 2012
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.925 0.120 2 21014672 intron variant G/A;T snv 0.700 1.000 2 2012 2012
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 0.925 0.120 2 21014672 intron variant G/A;T snv 0.700 1.000 1 2012 2012
elevated blood glucose level
CUI: C0495706
Disease: elevated blood glucose level
111 0.925 0.120 2 21014672 intron variant G/A;T snv 0.700 1.000 1 2009 2009
Glucose measurement
CUI: C0337438
Disease: Glucose measurement
111 0.925 0.120 2 21014672 intron variant G/A;T snv 0.700 1.000 1 2009 2009
Lipids measurement
CUI: C0523744
Disease: Lipids measurement
53 0.925 0.120 2 21014672 intron variant G/A;T snv 0.700 1.000 1 2009 2009
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.925 0.120 2 21014672 intron variant G/A;T snv 0.700 1.000 1 2012 2012
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 0.925 0.120 2 21014672 intron variant G/A;T snv 0.700 1.000 1 2012 2012
Avascular Necrosis of Femur Head
CUI: C0410480
Disease: Avascular Necrosis of Femur Head
20 0.925 0.120 2 21014672 intron variant G/A;T snv 0.010 1.000 1 2015 2015
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.925 0.120 2 21014672 intron variant G/A;T snv 0.010 1.000 1 2018 2018