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 0.700 1.000 1 2010 2010
dbSNP: rs11064010
rs11064010
VWF
2 12 6050980 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs112814955
rs112814955
VWF
1 12 6116765 intron variant G/A snv 5.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs216303
rs216303
VWF
1 12 6049879 intron variant C/T snv 0.89 0.700 1.000 1 2016 2016
dbSNP: rs2238109
rs2238109
VWF
2 12 6044801 intron variant T/A snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs2283335
rs2283335
VWF
1 12 6048228 intron variant T/C snv 0.40 0.700 1.000 1 2019 2019