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: rs752411521
rs752411521
CBFA2T2
1 1.000 0.040 20 33624825 missense variant T/C snv 4.0E-06 0.010 1.000 1 2002 2002