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 0.851 0.120 2 43845437 intron variant G/C;T snv 0.800 1.000 9 2010 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.851 0.120 2 43845437 intron variant G/C;T snv 0.800 1.000 5 2010 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.851 0.120 2 43845437 intron variant G/C;T snv 0.710 1.000 3 2015 2018
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 0.851 0.120 2 43845437 intron variant G/C;T snv 0.700 1.000 4 2010 2013
Alcohol consumption
CUI: C0001948
Disease: Alcohol consumption
535 0.851 0.120 2 43845437 intron variant G/C;T snv 0.700 1.000 1 2019 2019
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.851 0.120 2 43845437 intron variant G/C;T snv 0.700 1.000 1 2019 2019
Cholecystolithiasis
CUI: C0947622
Disease: Cholecystolithiasis
62 0.851 0.120 2 43845437 intron variant G/C;T snv 0.700 1.000 1 2007 2007
Cholelithiasis
CUI: C0008350
Disease: Cholelithiasis
90 0.851 0.120 2 43845437 intron variant G/C;T snv 0.700 1.000 1 2007 2007
Lipids measurement
CUI: C0523744
Disease: Lipids measurement
53 0.851 0.120 2 43845437 intron variant G/C;T snv 0.700 1.000 1 2009 2009
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.851 0.120 2 43845437 intron variant G/C;T snv 0.700 1.000 1 2012 2012
Gall Bladder Diseases
CUI: C0016977
Disease: Gall Bladder Diseases
4 0.851 0.120 2 43845437 intron variant G/C;T snv 0.010 1.000 1 2016 2016