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: rs587777067
rs587777067
DDX59
1 1.000 0.080 1 200650639 missense variant A/C;T snv 1.2E-05 0.800 1.000 1 2013 2013
dbSNP: rs886037652
rs886037652
DDX59
1 1.000 0.080 1 200644514 missense variant C/T snv 0.800 1.000 1 2013 2013