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: rs118203907
rs118203907
F5
3 0.882 0.080 1 169530805 missense variant T/C snv 1.6E-05 1.4E-05 0.810 1.000 6 2000 2011
dbSNP: rs118203910
rs118203910
F5
1 1.000 0.080 1 169518453 missense variant G/A snv 8.0E-06 0.800 1.000 2 2011 2019
dbSNP: rs6025
rs6025
F5
43 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.700 1.000 3 1994 1994
dbSNP: rs757953549
rs757953549
F5
1 1.000 0.080 1 169542872 stop gained G/A;T snv 4.0E-06 0.700 1.000 3 1998 2012
dbSNP: rs747006175
rs747006175
F5
1 1.000 0.080 1 169550715 missense variant G/A snv 5.2E-05 2.1E-05 0.700 1.000 1 2019 2019
dbSNP: rs118203908
rs118203908
F5
1 1.000 0.080 1 169542689 stop gained G/A;T snv 0.700 0
dbSNP: rs118203909
rs118203909
F5
1 1.000 0.080 1 169541609 stop gained G/A snv 4.0E-06 7.0E-06 0.700 0