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: rs1800297
rs1800297
F8
1 1.000 0.080 X 154860563 missense variant T/C snv 2.0E-02 7.3E-02 0.010 1.000 1 2015 2015