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: rs11024102
rs11024102
0.851 0.040 11 16987058 intron variant T/C snv 0.20
CUI: C0017606
Disease: Primary angle-closure glaucoma
Primary angle-closure glaucoma
Eye Diseases 0.790 0.900 10 2013 2019
dbSNP: rs4141194
rs4141194
11 16989629 intron variant C/A snv 0.20
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 3 2018 2018
dbSNP: rs381815
rs381815
1.000 0.040 11 16880721 intron variant C/A;T snv 0.24
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 2 2009 2017
dbSNP: rs381815
rs381815
1.000 0.040 11 16880721 intron variant C/A;T snv 0.24
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement
0.700 1.000 2 2009 2011
dbSNP: rs416258
rs416258
11 16890089 intron variant G/C snv 0.29
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 2 2018 2019
dbSNP: rs11024074
rs11024074
0.925 0.040 11 16895672 intron variant T/C snv 0.29
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs11024074
rs11024074
0.925 0.040 11 16895672 intron variant T/C snv 0.29
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2009 2009
dbSNP: rs11024074
rs11024074
0.925 0.040 11 16895672 intron variant T/C snv 0.29
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs11024074
rs11024074
0.925 0.040 11 16895672 intron variant T/C snv 0.29
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs11024074
rs11024074
0.925 0.040 11 16895672 intron variant T/C snv 0.29
Diastolic blood pressure measurement
0.700 1.000 1 2009 2009
dbSNP: rs11024102
rs11024102
0.851 0.040 11 16987058 intron variant T/C snv 0.20
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle
Eye Diseases 0.700 1.000 1 2012 2012
dbSNP: rs11024102
rs11024102
0.851 0.040 11 16987058 intron variant T/C snv 0.20
CUI: C0017601
Disease: Glaucoma
Glaucoma
Eye Diseases 0.700 1.000 1 2012 2012
dbSNP: rs11024102
rs11024102
0.851 0.040 11 16987058 intron variant T/C snv 0.20
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2018 2018
dbSNP: rs177542
rs177542
11 16901107 intron variant G/A snv 0.47
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2017 2017
dbSNP: rs381815
rs381815
1.000 0.040 11 16880721 intron variant C/A;T snv 0.24
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs381815
rs381815
1.000 0.040 11 16880721 intron variant C/A;T snv 0.24
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2017 2017
dbSNP: rs381815
rs381815
1.000 0.040 11 16880721 intron variant C/A;T snv 0.24
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2011 2011
dbSNP: rs381815
rs381815
1.000 0.040 11 16880721 intron variant C/A;T snv 0.24
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs382280
rs382280
11 16836252 intron variant C/T snv 9.3E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs407354
rs407354
11 16865345 intron variant C/T snv 8.7E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs414992
rs414992
11 16872543 intron variant C/T snv 0.13
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs416258
rs416258
11 16890089 intron variant G/C snv 0.29
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs416258
rs416258
11 16890089 intron variant G/C snv 0.29
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs448671
rs448671
11 16878556 intron variant T/G snv 0.24
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs448671
rs448671
11 16878556 intron variant T/G snv 0.24
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2018 2018