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: rs11774829
rs11774829
ZFPM2
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: rs11774829
rs11774829
ZFPM2
8 104966140 intron variant T/A snv 7.6E-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
dbSNP: rs11774829
rs11774829
ZFPM2
8 104966140 intron variant T/A snv 7.6E-02
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs12546444
rs12546444
ZFPM2
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
ZFPM2
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
ZFPM2
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
ZFPM2
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
ZFPM2
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
ZFPM2
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
ZFPM2
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
ZFPM2
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
ZFPM2
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: rs284489
rs284489
ZFPM2
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: rs284491
rs284491
ZFPM2
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
ZFPM2
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
ZFPM2
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: rs57942103
rs57942103
ZFPM2
1.000 0.040 8 105501233 intron variant A/C snv 0.25
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs57942103
rs57942103
ZFPM2
1.000 0.040 8 105501233 intron variant A/C snv 0.25
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.700 1.000 1 2019 2019
dbSNP: rs57942103
rs57942103
ZFPM2
1.000 0.040 8 105501233 intron variant A/C snv 0.25
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE 		0.700 1.000 1 2019 2019
dbSNP: rs72679151
rs72679151
ZFPM2
8 104614889 intron variant C/T snv 0.17
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7819593
rs7819593
ZFPM2
8 105102944 intron variant T/C snv 0.35
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.700 1.000 1 2019 2019
dbSNP: rs7837523
rs7837523
ZFPM2
8 105517074 intron variant A/T snv 0.80
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs9297357
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.700 1.000 1 2013 2013
dbSNP: rs9297357
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2013 2013
dbSNP: rs9297357
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.800 1.000 1 2013 2013