Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6993770
rs6993770
0.925 0.080 8 105569300 intron variant A/T snv 0.31
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.800 1.000 4 2011 2019
dbSNP: rs6993770
rs6993770
0.925 0.080 8 105569300 intron variant A/T snv 0.31
Vascular Endothelial Growth Factor Measurement
0.800 1.000 2 2011 2016
dbSNP: rs284489
rs284489
0.882 0.080 8 104945792 intron variant A/G snv 0.45
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle
0.800 1.000 1 2012 2012
dbSNP: rs9297357
rs9297357
0.851 0.040 8 105130105 intron variant C/G;T snv
Attention deficit hyperactivity disorder
0.800 1.000 1 2013 2013
dbSNP: rs11774829
rs11774829
8 104966140 intron variant T/A snv 7.6E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 2 2019 2019
dbSNP: rs4602861
rs4602861
8 105578478 intron variant A/G;T snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 2 2015 2017
dbSNP: rs10093110
rs10093110
1.000 0.040 8 105553186 intron variant G/A;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2018 2018
dbSNP: rs11774829
rs11774829
8 104966140 intron variant T/A snv 7.6E-02
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs11774829
rs11774829
8 104966140 intron variant T/A snv 7.6E-02
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs12546444
rs12546444
1.000 0.080 8 105346392 intron variant A/T snv 8.0E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.700 1.000 1 2017 2017
dbSNP: rs12678719
rs12678719
1.000 8 105503826 intron variant C/G snv 0.37
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval
0.700 1.000 1 2018 2018
dbSNP: rs1350723
rs1350723
8 105218944 intron variant G/A snv 0.69
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs1375961
rs1375961
8 105535755 intron variant T/G snv 0.14
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs1383592
rs1383592
8 105418448 intron variant G/A snv 0.26
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs1460583
rs1460583
1.000 0.040 8 105096365 intron variant T/C snv 0.26
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 1 2019 2019
dbSNP: rs16872085
rs16872085
8 104945312 intron variant A/G snv 7.6E-02
CUI: C0085298
Disease: Sudden Cardiac Death
Sudden Cardiac Death
0.700 1.000 1 2011 2011
dbSNP: rs17210179
rs17210179
8 105333241 intron variant C/T snv 0.11
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs2342781
rs2342781
1.000 0.040 8 105253492 intron variant C/G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2018 2018
dbSNP: rs2343592
rs2343592
8 105560042 intron variant A/G snv 0.30
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.700 1.000 1 2018 2018
dbSNP: rs28416651
rs28416651
1.000 0.040 8 105552424 intron variant G/A;C snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2018 2018
dbSNP: rs284491
rs284491
0.925 0.040 8 104946405 intron variant C/T snv 0.45
CUI: C0152136
Disease: Low Tension Glaucoma
Low Tension Glaucoma
0.700 1.000 1 2016 2016
dbSNP: rs35783704
rs35783704
8 104954030 intron variant G/A snv 7.2E-02
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019
dbSNP: rs35783704
rs35783704
8 104954030 intron variant G/A snv 7.2E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2017 2017
dbSNP: rs3832566
rs3832566
8 105561297 intron variant A/- delins 0.29
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1.000 1 2016 2016
dbSNP: rs4541868
rs4541868
8 105578477 intron variant C/A snv 0.33
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.700 1.000 1 2019 2019