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: rs1800595
rs1800595
F5
2 0.925 0.080 1 169541110 missense variant T/C;G snv 5.7E-02 0.010 1.000 1 2012 2012
dbSNP: rs6025
rs6025
F5
43 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.010 1.000 1 2012 2012