rs886126, CUX2

N. diseases: 1
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 1.000 0.040 12 111241410 intron variant C/T snv 0.34 0.800 1.000 1 2013 2013