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: rs387906655
rs387906655
MOG
1 1.000 6 29659628 missense variant C/G snv 0.800 1.000 1 2011 2011