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.
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
62 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.820 0.500 4 2010 2016
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
923 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.800 16 2008 2017
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
814 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.800 6 2010 2017
Uric acid measurement (procedure)
CUI: C0202239
Disease: Uric acid measurement (procedure)
2331 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.800 5 2009 2016
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
11 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.800 3 2010 2013
Glomerular filtration rate finding
CUI: C1561549
Disease: Glomerular filtration rate finding
144 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.800 3 2013 2017
C-reactive protein measurement
CUI: C0201657
Disease: C-reactive protein measurement
245 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.800 3 2011 2017
Platelet Count measurement
CUI: C0032181
Disease: Platelet Count measurement
353 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.800 2 2011 2017
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
3393 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.800 2 2012 2012
Protein measurement
CUI: C0202202
Disease: Protein measurement
422 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.800 2 2012 2016
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
120 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.800 2 2010 2012
Serum gamma-glutamyl transferase measurement
44 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.800 1 2011 2011
Glucose tolerance test
CUI: C0017741
Disease: Glucose tolerance test
19 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.800 1 2010 2010
FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 5
2 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 4 2008 2010
Creatinine measurement, serum (procedure)
140 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 2 2010 2016
Gout
CUI: C0018099
Disease: Gout
90 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 2 2016 2017
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
451 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 2 2016 2017
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
956 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 2 2017 2017
Protein C measurement
CUI: C0919677
Disease: Protein C measurement
514 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 1 2010 2010
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
212 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 1 2017 2017
Waist Circumference
CUI: C0455829
Disease: Waist Circumference
227 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 1 2008 2008
Cholecystolithiasis
CUI: C0947622
Disease: Cholecystolithiasis
58 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 1 2017 2017
Red cell distribution width determination
206 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 1 2017 2017
Eosinophil count result
CUI: C0750879
Disease: Eosinophil count result
419 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 1 2017 2017
Granulocyte count
CUI: C0857490
Disease: Granulocyte count
150 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.700 1 2017 2017