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: rs7914558
rs7914558
CNNM2
0.851 0.040 10 103016151 intron variant G/A snv 0.40
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.830 1.000 2 2011 2020
dbSNP: rs12413409
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.800 1.000 2 2011 2014
dbSNP: rs12413409
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm 		0.800 1.000 1 2010 2010
dbSNP: rs1890185
rs1890185
CNNM2
10 102988961 intron variant A/G snv 0.41
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		0.800 1.000 1 2013 2013
dbSNP: rs7914558
rs7914558
CNNM2
0.851 0.040 10 103016151 intron variant G/A snv 0.40
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.800 1.000 1 2013 2013
dbSNP: rs11191548
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.780 1.000 1 2011 2018
dbSNP: rs11191548
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 8 2009 2018
dbSNP: rs11191548
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 3 2011 2018
dbSNP: rs10786736
rs10786736
NT5C2 ; CNNM2
1.000 0.040 10 103089359 3 prime UTR variant G/C snv 9.9E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 2 2017 2019
dbSNP: rs55833108
rs55833108
CNNM2
1.000 0.040 10 102981826 intron variant G/T snv 0.14
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 2 2015 2019
dbSNP: rs1046411
rs1046411
CNNM2
10 103078059 3 prime UTR variant G/A snv 0.32
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs111326718
rs111326718
CNNM2
10 103011454 intron variant -/TAAAA delins 0.40
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs11191514
rs11191514
CNNM2
10 103013607 intron variant C/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2015 2015
dbSNP: rs11191548
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs12260436
rs12260436
CNNM2
1.000 0.040 10 102981357 intron variant A/C snv 0.29
CUI: C0003467
Disease: Anxiety
Anxiety 		0.700 1.000 1 2018 2018
dbSNP: rs12414777
rs12414777
CNNM2
1.000 0.040 10 102938024 intron variant C/G;T snv 0.20
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
dbSNP: rs12783467
rs12783467
CNNM2
10 102948555 intron variant A/G snv 0.21
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2018 2018
dbSNP: rs140473396
rs140473396
CNNM2
10 103036129 intron variant ACACACAC/-;AC;ACAC;ACACAC;ACACACACAC;ACACACACACAC;ACACACACACACAC;ACACACACACACACAC delins
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs1890184
rs1890184
CNNM2
1.000 0.040 10 102988702 intron variant A/C;T snv
CUI: C0003467
Disease: Anxiety
Anxiety 		0.700 1.000 1 2018 2018
dbSNP: rs200510190
rs200510190
CNNM2
10 103031838 intron variant C/- del 0.41
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs200510190
rs200510190
CNNM2
10 103031838 intron variant C/- del 0.41
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs7092200
rs7092200
CNNM2
10 103085115 3 prime UTR variant T/C snv 0.42
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs7914558
rs7914558
CNNM2
0.851 0.040 10 103016151 intron variant G/A snv 0.40
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2013 2013
dbSNP: rs7914558
rs7914558
CNNM2
0.851 0.040 10 103016151 intron variant G/A snv 0.40
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.700 1.000 1 2013 2013
dbSNP: rs7914558
rs7914558
CNNM2
0.851 0.040 10 103016151 intron variant G/A snv 0.40
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2013 2013