Source: CURATED

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: rs387906975
rs387906975
CNNM2
1.000 10 103049788 missense variant C/T snv
CUI: C3151295
Disease: HYPOMAGNESEMIA 6, RENAL
HYPOMAGNESEMIA 6, RENAL 		0.800 1.000 1 2011 2011
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: rs794726858
rs794726858
CNNM2 ; LOC107984265
1.000 10 102919286 missense variant C/G snv
CUI: C4225333
Disease: HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION
HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION 		0.800 1.000 1 2014 2014
dbSNP: rs786205909
rs786205909
CNNM2 ; LOC107984265
1.000 10 102918844 missense variant G/A snv 4.9E-06
CUI: C4225333
Disease: HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION
HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION 		0.800 0
dbSNP: rs786205910
rs786205910
CNNM2 ; LOC107984265
1.000 10 102919549 missense variant G/A snv
CUI: C4225333
Disease: HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION
HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION 		0.800 0
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: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 3 2011 2011
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: rs11191548
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement 		0.700 1.000 2 2009 2011
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: rs11191548
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2011 2011
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: rs12411886
rs12411886
CNNM2
0.882 0.080 10 102925542 intron variant C/A snv 7.8E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2009 2009
dbSNP: rs12411886
rs12411886
CNNM2
0.882 0.080 10 102925542 intron variant C/A snv 7.8E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2011 2011
dbSNP: rs12411886
rs12411886
CNNM2
0.882 0.080 10 102925542 intron variant C/A snv 7.8E-02
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm 		0.700 1.000 1 2010 2010