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
447 1.000 0.036 15 90894158 intron variant A/C,T snp 6.4E-05; 0.28 0.800 1 2012 2012
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
244 1.000 0.036 15 90894158 intron variant A/C,T snp 6.4E-05; 0.28 0.700 3 2012 2017
Blood Pressure
CUI: C0005823
Disease: Blood Pressure
223 1.000 0.036 15 90894158 intron variant A/C,T snp 6.4E-05; 0.28 0.700 2 2011 2012
Blood pressure finding
CUI: C1271104
Disease: Blood pressure finding
223 1.000 0.036 15 90894158 intron variant A/C,T snp 6.4E-05; 0.28 0.700 2 2011 2012
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
256 1.000 0.036 15 90894158 intron variant A/C,T snp 6.4E-05; 0.28 0.700 2 2012 2017
Systemic arterial pressure
CUI: C1272641
Disease: Systemic arterial pressure
223 1.000 0.036 15 90894158 intron variant A/C,T snp 6.4E-05; 0.28 0.700 2 2011 2012
Mean blood pressure
CUI: C0428886
Disease: Mean blood pressure
62 1.000 0.036 15 90894158 intron variant A/C,T snp 6.4E-05; 0.28 0.700 1 2011 2011
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
454 1.000 0.036 15 90894158 intron variant A/C,T snp 6.4E-05; 0.28 0.700 1 2015 2015