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: rs61750581
rs61750581
VWF
2 0.925 0.080 12 6018581 missense variant A/G snv 0.700 1.000 20 1991 2012
dbSNP: rs61750584
rs61750584
VWF
3 0.882 0.080 12 6018535 missense variant A/G snv 0.700 1.000 20 1991 2012
dbSNP: rs61750588
rs61750588
VWF
2 0.925 0.080 12 6018506 missense variant C/G;T snv 0.700 1.000 20 1991 2012
dbSNP: rs61750590
rs61750590
VWF
2 0.925 0.080 12 6018476 missense variant G/A snv 0.700 1.000 20 1991 2012
dbSNP: rs61750596
rs61750596
VWF
2 0.925 0.080 12 6018424 missense variant A/T snv 0.700 1.000 20 1991 2012
dbSNP: rs61751310
rs61751310
VWF ; ANO2
3 0.882 0.080 12 5949140 missense variant A/G snv 0.700 1.000 20 1991 2012
dbSNP: rs63524161
rs63524161
VWF
2 0.925 0.080 12 6019603 missense variant C/A;G snv 0.700 1.000 20 1991 2012
dbSNP: rs41276738
rs41276738
VWF
7 0.807 0.080 12 6034812 missense variant C/T snv 3.4E-03 3.7E-03 0.810 1.000 1 2004 2004
dbSNP: rs61749368
rs61749368
VWF
1 1.000 0.080 12 6019726 missense variant T/C;G snv 1.4E-03; 1.4E-03 0.010 1.000 1 2013 2013
dbSNP: rs778661133
rs778661133
VWF
1 1.000 0.080 12 6018514 missense variant T/A snv 1.6E-05 0.010 1.000 1 2013 2013
dbSNP: rs267607326
rs267607326
VWF
2 0.925 0.080 12 6022841 missense variant T/C snv 0.700 0
dbSNP: rs267607353
rs267607353
VWF
1 1.000 0.080 12 6016197 missense variant A/C snv 1.4E-04 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