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: rs61749380
rs61749380
VWF
1 1.000 0.080 12 6019564 missense variant G/A;C snv 4.0E-06 0.710 1.000 1 2003 2003
dbSNP: rs61749398
rs61749398
VWF
2 0.925 0.080 12 6019448 missense variant C/T snv 8.0E-06 0.710 < 0.001 1 2006 2006
dbSNP: rs121964895
rs121964895
VWF
7 0.851 0.080 12 6021960 missense variant C/A;T snv 0.020 1.000 2 2000 2006
dbSNP: rs2228317
rs2228317
VWF
2 0.925 0.080 12 6046784 missense variant C/T snv 1.4E-02 5.6E-02 0.010 1.000 1 2006 2006
dbSNP: rs61749399
rs61749399
VWF
1 1.000 0.080 12 6019447 missense variant C/G snv 0.010 1.000 1 2002 2002