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: rs61749372
rs61749372
VWF
2 0.925 0.080 12 6019604 missense variant A/C;G snv 0.700 0
dbSNP: rs61750101
rs61750101
VWF
2 0.925 0.080 12 6018877 missense variant A/C snv 0.700 0
dbSNP: rs61750117
rs61750117
VWF
3 0.882 0.080 12 6018629 missense variant G/A;C;T snv 4.0E-06 0.700 0
dbSNP: rs61750579
rs61750579
VWF
2 0.925 0.080 12 6018598 missense variant A/T snv 0.700 0
dbSNP: rs61750581
rs61750581
VWF
2 0.925 0.080 12 6018581 missense variant A/G snv 0.700 0
dbSNP: rs61750584
rs61750584
VWF
3 0.882 0.080 12 6018535 missense variant A/G snv 0.700 0
dbSNP: rs61751310
rs61751310
VWF ; ANO2
3 0.882 0.080 12 5949140 missense variant A/G snv 0.700 0
dbSNP: rs61754010
rs61754010
VWF
3 0.882 0.080 12 6057995 missense variant T/C snv 4.0E-06 0.700 0
dbSNP: rs61754011
rs61754011
VWF
3 0.882 0.160 12 6057930 missense variant C/T snv 0.700 0
dbSNP: rs61750585
rs61750585
VWF
1 1.000 0.080 12 6018533 missense variant C/T snv 0.020 1.000 2 1999 2004
dbSNP: rs63524161
rs63524161
VWF
2 0.925 0.080 12 6019603 missense variant C/A;G snv 0.020 1.000 2 2004 2012
dbSNP: rs267607332
rs267607332
VWF
3 0.882 0.080 12 6022740 missense variant C/T snv 0.010 1.000 1 2004 2004
dbSNP: rs61749369
rs61749369
VWF
1 1.000 0.080 12 6019716 missense variant A/C snv 0.010 1.000 1 2006 2006
dbSNP: rs61750096
rs61750096
VWF
1 1.000 0.080 12 6018919 missense variant G/A;T snv 2.6E-04 0.010 1.000 1 2000 2000
dbSNP: rs61750097
rs61750097
VWF
2 0.925 0.080 12 6018910 missense variant A/C;G;T snv 0.010 < 0.001 1 2008 2008
dbSNP: rs61750596
rs61750596
VWF
2 0.925 0.080 12 6018424 missense variant A/T snv 0.010 1.000 1 2010 2010
dbSNP: rs772534075
rs772534075
VWF
1 1.000 0.080 12 6034819 stop gained G/A;C snv 4.0E-06; 3.2E-05 0.010 1.000 1 1993 1993