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: rs2074356
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 2 2012 2013