Source: INFERRED ×
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: rs1057519767
rs1057519767
FLT3
1 1.000 0.040 13 28028205 missense variant T/C snv 0.700 1.000 3 2012 2014