rs12413409, CNNM2

N. diseases: 6
Source: GWASDB ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
388 0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 0.800 1.000 1 2011 2014
Intracranial Aneurysm
CUI: C0007766
Disease: Intracranial Aneurysm
19 0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 0.800 1.000 1 2010 2010
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
107 0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 0.700 1.000 1 2014 2014
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
32 0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 0.700 1.000 1 2013 2013
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
224 0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 0.700 1.000 1 2009 2009
Systolic blood pressure measurement
CUI: C1306620
Disease: Systolic blood pressure measurement
35 0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 0.700 1.000 1 2013 2013