rs12411886, CNNM2

N. diseases: 3
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 0.882 0.080 10 102925542 intron variant C/A snv 7.8E-02 0.700 1.000 1 2011 2011
Intracranial Aneurysm
CUI: C0007766
Disease: Intracranial Aneurysm
19 0.882 0.080 10 102925542 intron variant C/A snv 7.8E-02 0.700 1.000 1 2010 2010
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
224 0.882 0.080 10 102925542 intron variant C/A snv 7.8E-02 0.700 1.000 1 2009 2009