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: rs2434237
rs2434237
CPLX2
1.000 0.080 5 175797902 intron variant C/A snv 0.18
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.700 1.000 1 2011 2011