rs2954029, None

N. diseases: 7
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.
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
744 0.807 0.160 8 125478730 intron variant A/T snv 0.42 0.800 1.000 6 2009 2019
High density lipoprotein measurement
681 0.807 0.160 8 125478730 intron variant A/T snv 0.42 0.800 1.000 4 2010 2019
Low density lipoprotein cholesterol measurement
555 0.807 0.160 8 125478730 intron variant A/T snv 0.42 0.800 1.000 4 2010 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
652 0.807 0.160 8 125478730 intron variant A/T snv 0.42 0.800 1.000 4 2010 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
107 0.807 0.160 8 125478730 intron variant A/T snv 0.42 0.800 1.000 1 2013 2018
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.807 0.160 8 125478730 intron variant A/T snv 0.42 0.700 1.000 4 2010 2013
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 0.807 0.160 8 125478730 intron variant A/T snv 0.42 0.700 1.000 4 2010 2013