rs673548, APOB

N. diseases: 7
Source: GWASCAT ×
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
837 0.925 0.120 2 21014672 intron variant G/A;T snv 0.800 1.000 3 2009 2019
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
951 0.925 0.120 2 21014672 intron variant G/A;T snv 0.800 1.000 2 2012 2019
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
731 0.925 0.120 2 21014672 intron variant G/A;T snv 0.800 1.000 1 2012 2018
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
124 0.925 0.120 2 21014672 intron variant G/A;T snv 0.800 1.000 1 2012 2012
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
766 0.925 0.120 2 21014672 intron variant G/A;T snv 0.800 1.000 1 2012 2018
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
84 0.925 0.120 2 21014672 intron variant G/A;T snv 0.700 1.000 1 2012 2012
Lipids measurement
CUI: C0523744
Disease: Lipids measurement
52 0.925 0.120 2 21014672 intron variant G/A;T snv 0.700 1.000 1 2009 2009