rs11066015, ACAD10

N. diseases: 5
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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03 0.800 1.000 1 2013 2013
Alcohol consumption
CUI: C0001948
Disease: Alcohol consumption
535 0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03 0.700 1.000 1 2013 2013
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03 0.700 1.000 1 2011 2011
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03 0.700 1.000 1 2011 2011
Uric acid measurement (procedure)
CUI: C0202239
Disease: Uric acid measurement (procedure)
1463 0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03 0.700 1.000 1 2018 2018