rs12140311, CLCNKB

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.
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 1.000 0.040 1 16052230 missense variant A/C;T snv 8.0E-06; 9.6E-02 0.030 0.667 3 2004 2011
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 1.000 0.040 1 16052230 missense variant A/C;T snv 8.0E-06; 9.6E-02 0.030 0.667 3 2005 2009
Tinnitus
CUI: C0040264
Disease: Tinnitus
14 1.000 0.040 1 16052230 missense variant A/C;T snv 8.0E-06; 9.6E-02 0.010 1.000 1 2006 2006