rs587777929, CCT7

N. diseases: 1
Source: ALL
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.
MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO
CUI: C1832662
Disease: MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO
3 2 73252803 missense variant C/T snv 2.0E-05 4.2E-05 0.700 1.000 1 2013 2013