Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2681492
rs2681492 		0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 3 2009 2018
dbSNP: rs2681492
rs2681492 		0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 2 2011 2013
dbSNP: rs2681492
rs2681492 		0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.710 1.000 2 2013 2018
dbSNP: rs2681492
rs2681492 		0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 2 2017 2018
dbSNP: rs11105368
rs11105368 		12 89680664 intron variant G/A;C snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.700 1.000 1 2017 2017
dbSNP: rs2681485
rs2681485 		12 89631845 intron variant G/A;T snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs2681485
rs2681485 		12 89631845 intron variant G/A;T snv
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2681485
rs2681485 		12 89631845 intron variant G/A;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs2681492
rs2681492 		0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs2681492
rs2681492 		0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs2681492
rs2681492 		0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs2681492
rs2681492 		0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement 		0.700 1.000 1 2009 2009
dbSNP: rs2681492
rs2681492 		0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs2681492
rs2681492 		0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs4842676
rs4842676 		12 89698005 intron variant G/C;T snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs7136259
rs7136259 		1.000 0.040 12 89687411 intron variant T/A;C;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.800 1.000 1 2012 2012
dbSNP: rs7136259
rs7136259 		1.000 0.040 12 89687411 intron variant T/A;C;G snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs7297206
rs7297206 		12 89625452 intron variant C/A;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs111337717
rs111337717 		12 89643729 intron variant T/C snv 3.9E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs111337717
rs111337717 		12 89643729 intron variant T/C snv 3.9E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs12818945
rs12818945 		1.000 0.040 12 89624457 intron variant C/A snv 4.5E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs12817819
rs12817819 		0.882 0.040 12 89645549 intron variant C/T snv 9.4E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs12817819
rs12817819 		0.882 0.040 12 89645549 intron variant C/T snv 9.4E-02
CUI: C0151744
Disease: Myocardial Ischemia
Myocardial Ischemia 		Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs12817819
rs12817819 		0.882 0.040 12 89645549 intron variant C/T snv 9.4E-02
CUI: C0745130
Disease: Resistant hypertensive disorder
Resistant hypertensive disorder 		Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs57481061
rs57481061 		1.000 0.040 12 89625401 intron variant C/G snv 0.14
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018