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: rs1063857
rs1063857
VWF
4 12 6044348 synonymous variant A/G snv 0.31 0.40 0.010 1.000 1 2011 2011
dbSNP: rs216293
rs216293
VWF
1 12 6044493 intron variant G/C;T snv 2.7E-04; 0.59 0.010 1.000 1 2011 2011
dbSNP: rs4764478
rs4764478
VWF
1 12 5968959 intron variant T/A snv 0.22 0.010 1.000 1 2011 2011