rs10803414, CLCNKB

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 1 16054087 intron variant C/T snv 0.40 0.010 1.000 1 2012 2012
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 1.000 0.040 1 16054087 intron variant C/T snv 0.40 0.010 1.000 1 2012 2012