rs2011616, EMILIN1

N. diseases: 2
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.
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 1.000 0.040 2 27079693 intron variant G/A snv 0.37 0.020 1.000 2 2009 2010
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 1.000 0.040 2 27079693 intron variant G/A snv 0.37 0.020 1.000 2 2009 2012