rs11221497, KCNJ5

N. diseases: 3
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.
Conn Syndrome
CUI: C1384514
Disease: Conn Syndrome
25 0.882 0.120 11 128890715 upstream gene variant G/C snv 0.19 0.010 1.000 1 2013 2013
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.882 0.120 11 128890715 upstream gene variant G/C snv 0.19 0.010 1.000 1 2013 2013
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.882 0.120 11 128890715 upstream gene variant G/C snv 0.19 0.010 1.000 1 2012 2012