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: rs121909091
rs121909091
DNM2
4 0.851 0.120 19 10798543 missense variant C/T snv 0.010 1.000 1 2010 2010