Source: BEFREE ×
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: rs137852237
rs137852237
F9
1 1.000 0.080 X 139551112 missense variant C/A;T snv 5.5E-06 0.810 1.000 1 2012 2016
dbSNP: rs137852249
rs137852249
F9
1 0.882 0.080 X 139561566 missense variant G/A snv 0.810 1.000 1 1989 2018
dbSNP: rs137852227
rs137852227
F9
1 0.925 0.080 X 139537144 stop gained C/T snv 0.710 1.000 1 1990 2016
dbSNP: rs137852248
rs137852248
F9
1 1.000 0.080 X 139561565 stop gained C/A;T snv 0.710 1.000 1 2012 2012
dbSNP: rs387906482
rs387906482
F9
2 1.000 0.080 X 139561716 missense variant T/C snv 9.4E-06 0.710 1.000 1 2000 2000
dbSNP: rs144314232
rs144314232
F9
1 1.000 0.080 X 139548430 synonymous variant G/A snv 5.5E-06 9.5E-06 0.010 1.000 1 2017 2017
dbSNP: rs147567879
rs147567879
F9
1 1.000 0.080 X 139561733 missense variant T/G snv 4.9E-05 0.010 1.000 1 2013 2013
dbSNP: rs371045754
rs371045754
F9
4 0.882 0.200 X 139530726 upstream gene variant A/C snv 5.5E-06 1.9E-05 0.010 1.000 1 2015 2015
dbSNP: rs753654616
rs753654616
F9
2 0.925 0.080 X 139561530 missense variant A/G snv 0.010 1.000 1 2011 2011