rs13306560, CLCN6;MTHFR

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.
Blood Pressure
CUI: C0005823
Disease: Blood Pressure
220 1.000 0.040 1 11806126 5 prime UTR variant C/T snv 3.7E-02 0.700 1.000 1 2010 2010
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 1.000 0.040 1 11806126 5 prime UTR variant C/T snv 3.7E-02 0.010 1.000 1 2015 2015
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 1.000 0.040 1 11806126 5 prime UTR variant C/T snv 3.7E-02 0.010 1.000 1 2015 2015