Source: GWASCAT

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: rs886126
rs886126
CUX2
1.000 0.040 12 111241410 intron variant C/T snv 0.34
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.800 1.000 1 2013 2013