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: rs61748470
rs61748470
VWF
1 1.000 0.080 12 6044420 missense variant C/A snv 0.010 1.000 1 2017 2017