rs45483293, HSD11B2

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.
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 1.000 0.040 16 67436012 synonymous variant G/A snv 3.1E-02 2.9E-02 0.020 0.500 2 1998 2005
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 1.000 0.040 16 67436012 synonymous variant G/A snv 3.1E-02 2.9E-02 0.010 1.000 1 2000 2000