rs11014166, CACNB2

N. diseases: 10
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
1085 0.882 0.040 10 18419869 intron variant A/T snv 0.27 0.800 1.000 1 2009 2009
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.882 0.040 10 18419869 intron variant A/T snv 0.27 0.710 1.000 2 2010 2011
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 0.882 0.040 10 18419869 intron variant A/T snv 0.27 0.700 1.000 2 2009 2017
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.882 0.040 10 18419869 intron variant A/T snv 0.27 0.700 1.000 2 2009 2017
Blood Pressure
CUI: C0005823
Disease: Blood Pressure
220 0.882 0.040 10 18419869 intron variant A/T snv 0.27 0.700 1.000 1 2011 2011
Diastolic blood pressure measurement
CUI: C1305849
Disease: Diastolic blood pressure measurement
81 0.882 0.040 10 18419869 intron variant A/T snv 0.27 0.700 1.000 1 2009 2009
Mean blood pressure
CUI: C0428886
Disease: Mean blood pressure
344 0.882 0.040 10 18419869 intron variant A/T snv 0.27 0.700 1.000 1 2016 2016
Systolic blood pressure measurement
CUI: C1306620
Disease: Systolic blood pressure measurement
95 0.882 0.040 10 18419869 intron variant A/T snv 0.27 0.700 1.000 1 2009 2009
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.882 0.040 10 18419869 intron variant A/T snv 0.27 0.010 1.000 1 2010 2010
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.882 0.040 10 18419869 intron variant A/T snv 0.27 0.010 1.000 1 2010 2010