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.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 0.800 1.000 3 2012 2017
Serum gamma-glutamyl transferase measurement
108 0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 0.800 1.000 1 2011 2011
Birth Weight
CUI: C0005612
Disease: Birth Weight
369 0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 0.700 1.000 1 2019 2019
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 0.700 1.000 1 2018 2018
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 0.700 1.000 1 2019 2019
Diabetes Mellitus, Insulin-Dependent
954 0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 0.700 1.000 1 2015 2015
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 0.700 1.000 1 2015 2015
Low density lipoprotein cholesterol measurement
1142 0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 0.700 1.000 1 2018 2018
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 0.700 1.000 1 2018 2018
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 0.700 1.000 1 2018 2018