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: rs61749389
rs61749389
VWF
1 1.000 0.080 12 6019493 missense variant T/C snv 0.700 0
dbSNP: rs762105711
rs762105711
VWF
1 1.000 0.080 12 6025623 frameshift variant C/- del 0.700 0
dbSNP: rs146698837
rs146698837
F7
2 0.925 0.080 13 113118584 missense variant G/A snv 6.0E-05 5.6E-05 0.010 1.000 1 1992 1992
dbSNP: rs61754010
rs61754010
VWF
3 0.882 0.080 12 6057995 missense variant T/C snv 4.0E-06 0.010 1.000 1 1998 1998
dbSNP: rs61749403
rs61749403
VWF
3 0.882 0.080 12 6019396 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 1999 1999
dbSNP: rs61753997
rs61753997
VWF
3 0.882 0.080 12 6075392 missense variant G/A snv 2.8E-05; 8.0E-06 4.2E-05 0.010 1.000 1 2000 2000
dbSNP: rs61751310
rs61751310
VWF ; ANO2
3 0.882 0.080 12 5949140 missense variant A/G snv 0.010 1.000 1 2001 2001
dbSNP: rs976240876
rs976240876
VWF
1 1.000 0.080 12 6056863 missense variant G/A;C snv 1.8E-05 7.0E-06 0.010 1.000 1 2001 2001
dbSNP: rs61748466
rs61748466
VWF
1 1.000 0.080 12 6046726 missense variant G/A snv 1.6E-05 1.4E-05 0.010 1.000 1 2003 2003
dbSNP: rs61750097
rs61750097
VWF
2 0.925 0.080 12 6018910 missense variant A/C;G;T snv 0.010 1.000 1 2004 2004
dbSNP: rs1800386
rs1800386
VWF
5 0.851 0.120 12 6018667 missense variant T/C snv 2.7E-03 2.3E-03 0.710 1.000 1 2005 2005
dbSNP: rs267607369
rs267607369
VWF ; ANO2
1 1.000 0.080 12 5949055 missense variant G/A;T snv 0.010 1.000 1 2006 2006
dbSNP: rs61750610
rs61750610
VWF
3 0.925 0.080 12 6013630 missense variant G/T snv 0.010 1.000 1 2006 2006
dbSNP: rs61750588
rs61750588
VWF
2 0.925 0.080 12 6018506 missense variant C/G;T snv 0.010 1.000 1 2007 2007
dbSNP: rs61750590
rs61750590
VWF
2 0.925 0.080 12 6018476 missense variant G/A snv 0.010 1.000 1 2007 2007
dbSNP: rs61751286
rs61751286
VWF
1 1.000 0.080 12 5976158 missense variant G/A snv 8.0E-05 1.3E-04 0.700 1.000 3 2007 2009
dbSNP: rs1188383936
rs1188383936
F2
102 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs1217691063
rs1217691063
MTHFR
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs1255283120
rs1255283120
MTHFR
7 0.807 0.160 1 11792345 missense variant G/A snv 4.0E-06 7.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs61748482
rs61748482
VWF
1 1.000 0.080 12 6034813 missense variant G/A snv 2.0E-05 7.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs61749385
rs61749385
VWF
2 0.925 0.080 12 6019501 missense variant C/A;T snv 0.010 1.000 1 2010 2010
dbSNP: rs782261759
rs782261759
ADAMTS13 ; CACFD1
1 1.000 0.080 9 133458978 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs899127658
rs899127658
F2
82 0.547 0.720 11 46739084 missense variant G/A;C snv 0.010 1.000 1 2010 2010
dbSNP: rs267607324
rs267607324
VWF
2 0.925 0.080 12 6022889 missense variant C/A snv 0.020 1.000 2 2008 2011
dbSNP: rs61751311
rs61751311
VWF ; ANO2
1 1.000 0.080 12 5949139 missense variant C/G snv 0.010 1.000 1 2012 2012