rs3846663, HMGCR;CERT1

N. diseases: 7
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.
Low density lipoprotein cholesterol measurement
1142 0.882 0.120 5 75359901 intron variant C/T snv 0.35 0.800 1.000 3 2009 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.882 0.120 5 75359901 intron variant C/T snv 0.35 0.700 1.000 1 2011 2011
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 0.882 0.120 5 75359901 intron variant C/T snv 0.35 0.700 1.000 1 2009 2009
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.882 0.120 5 75359901 intron variant C/T snv 0.35 0.700 1.000 1 2019 2019
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.882 0.120 5 75359901 intron variant C/T snv 0.35 0.700 1.000 1 2009 2009
Obesity
CUI: C0028754
Disease: Obesity
1111 0.882 0.120 5 75359901 intron variant C/T snv 0.35 0.010 1.000 1 2014 2014
Overweight and obesity
CUI: C1561826
Disease: Overweight and obesity
29 0.882 0.120 5 75359901 intron variant C/T snv 0.35 0.010 1.000 1 2014 2014