rs12654264, HMGCR

N. diseases: 5
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.
Low density lipoprotein cholesterol measurement
555 0.925 0.120 5 75352778 intron variant A/T snv 0.38 0.800 1.000 2 2008 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
652 0.925 0.120 5 75352778 intron variant A/T snv 0.38 0.800 1.000 1 2012 2019
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 0.925 0.120 5 75352778 intron variant A/T snv 0.38 0.700 1.000 2 2008 2012
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
388 0.925 0.120 5 75352778 intron variant A/T snv 0.38 0.700 1.000 1 2011 2011
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3265 0.925 0.120 5 75352778 intron variant A/T snv 0.38 0.700 1.000 1 2011 2011