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: rs17080102
rs17080102 		6 150683634 5 prime UTR variant G/C snv 8.6E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 6 2013 2019
dbSNP: rs17080102
rs17080102 		6 150683634 5 prime UTR variant G/C snv 8.6E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 4 2013 2018
dbSNP: rs113397083
rs113397083 		6 150663605 non coding transcript exon variant G/A snv 8.2E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs12663498
rs12663498 		1.000 0.040 6 150682704 intron variant C/T snv 9.3E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs17080091
rs17080091 		1.000 0.040 6 150676265 intron variant C/T snv 0.11
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs17080093
rs17080093 		6 150676304 intron variant C/T snv 0.12
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2016 2016
dbSNP: rs17080093
rs17080093 		6 150676304 intron variant C/T snv 0.12
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2016 2016
dbSNP: rs17080102
rs17080102 		6 150683634 5 prime UTR variant G/C snv 8.6E-02
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2013 2013
dbSNP: rs62434109
rs62434109 		6 150654176 intron variant T/G snv 8.4E-02
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement 		0.700 1.000 1 2018 2018
dbSNP: rs62434109
rs62434109 		6 150654176 intron variant T/G snv 8.4E-02
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs62434109
rs62434109 		6 150654176 intron variant T/G snv 8.4E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs62434109
rs62434109 		6 150654176 intron variant T/G snv 8.4E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs62434109
rs62434109 		6 150654176 intron variant T/G snv 8.4E-02
CUI: C1305849
Disease: Diastolic blood pressure measurement
Diastolic blood pressure measurement 		0.700 1.000 1 2018 2018
dbSNP: rs62434111
rs62434111 		6 150656822 intron variant C/A snv 8.3E-02
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs62434120
rs62434120 		6 150671234 intron variant T/A snv 9.8E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2017 2017
dbSNP: rs62434120
rs62434120 		6 150671234 intron variant T/A snv 9.8E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.700 1.000 1 2017 2017
dbSNP: rs62434120
rs62434120 		6 150671234 intron variant T/A snv 9.8E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2017 2017
dbSNP: rs62434129
rs62434129 		6 150687701 intron variant A/G;T snv 8.8E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs62434129
rs62434129 		6 150687701 intron variant A/G;T snv 8.8E-02
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs62434129
rs62434129 		6 150687701 intron variant A/G;T snv 8.8E-02
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs62434129
rs62434129 		6 150687701 intron variant A/G;T snv 8.8E-02
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs62434129
rs62434129 		6 150687701 intron variant A/G;T snv 8.8E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs62434129
rs62434129 		6 150687701 intron variant A/G;T snv 8.8E-02
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019