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: rs61750630
rs61750630
VWF
2 0.925 0.080 12 5981988 missense variant C/A snv 0.060 1.000 6 2000 2015
dbSNP: rs61750584
rs61750584
VWF
3 0.882 0.080 12 6018535 missense variant A/G snv 0.700 1.000 8 1991 2019
dbSNP: rs41276738
rs41276738
VWF
7 0.807 0.080 12 6034812 missense variant C/T snv 3.4E-03 3.7E-03 0.710 1.000 16 1991 2019