rs13333226, UMOD

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.
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
447 0.923 0.071 16 20354332 intron variant A/G snp 0.22 0.810 1.000 1 2011 2011
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
126 0.923 0.071 16 20354332 intron variant A/G snp 0.22 0.700 0
Diabetes
CUI: C0011847
Disease: Diabetes
349 0.923 0.071 16 20354332 intron variant A/G snp 0.22 0.010 1.000 1 2011 2011
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
440 0.923 0.071 16 20354332 intron variant A/G snp 0.22 0.010 1.000 1 2011 2011
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
93 0.923 0.071 16 20354332 intron variant A/G snp 0.22 0.010 1.000 1 2011 2011