rs145044782, GLCCI1

N. diseases: 2
Source: ALL
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.
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.925 0.040 7 7995866 intron variant G/A snv 2.9E-02 0.700 1.000 1 2017 2017
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.925 0.040 7 7995866 intron variant G/A snv 2.9E-02 0.700 1.000 1 2017 2017