Gene: VWF ×
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: rs216321
rs216321
VWF
1 1.000 0.080 12 6034818 missense variant T/C snv 0.90 0.92 0.010 1.000 1 1999 1999