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: rs376588714
rs376588714
FLT3
1 1.000 0.040 13 28018483 missense variant T/C snv 2.4E-05 1.4E-05 0.710 1.000 4 2005 2014