Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs587777052
rs587777052
EEF2
1 1.000 0.080 19 3978099 missense variant G/T snv 0.800 1.000 2 2010 2012