Source: GWASDB

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: rs6725887
rs6725887
WDR12
0.851 0.080 2 202881162 intron variant T/C snv 8.9E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.800 1.000 2 2011 2014