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: rs397514711
rs397514711
IRF8
1 1.000 16 85909053 missense variant A/G snv 0.810 1.000 2 2011 2013