rs2544390, LRP2

N. diseases: 4
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.
Uric acid measurement (procedure)
CUI: C0202239
Disease: Uric acid measurement (procedure)
1463 0.925 0.080 2 169348336 intron variant C/T snv 0.45 0.700 1.000 1 2010 2010
Hyperuricemia
CUI: C0740394
Disease: Hyperuricemia
76 0.925 0.080 2 169348336 intron variant C/T snv 0.45 0.010 1.000 1 2013 2013
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.925 0.080 2 169348336 intron variant C/T snv 0.45 0.010 1.000 1 2015 2015
Neural Tube Defects
CUI: C0027794
Disease: Neural Tube Defects
122 0.925 0.080 2 169348336 intron variant C/T snv 0.45 0.010 1.000 1 2018 2018