rs673548, APOB

N. diseases: 10
Source: GWASDB ×
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
CUI: C0392885
Disease: High density lipoprotein measurement
681 0.925 0.120 2 21014672 intron variant G/A;T snv 0.800 1.000 2 2012 2019
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
744 0.925 0.120 2 21014672 intron variant G/A;T snv 0.800 1.000 2 2009 2019
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
555 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
48 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
652 0.925 0.120 2 21014672 intron variant G/A;T snv 0.800 1.000 1 2012 2018
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
elevated blood glucose level
CUI: C0495706
Disease: elevated blood glucose level
48 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
48 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
3265 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