Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61749397
VWF
0.807 0.080 12 6019472 missense variant C/G;T snv 4.0E-06 9
rs41276738
VWF
0.807 0.080 12 6034812 missense variant C/T snv 3.4E-03 3.7E-03 7
rs61749384
VWF
0.882 0.080 12 6019502 missense variant G/A snv 5
rs61749370
VWF
0.882 0.080 12 6019621 missense variant G/A;T snv 8.0E-04; 2.8E-04 3
rs61749387
VWF
0.882 0.080 12 6019496 missense variant G/A snv 3
rs61749403
VWF
0.882 0.080 12 6019396 missense variant C/A;G;T snv 4.0E-06 3
rs61750070
VWF
0.882 0.080 12 6019303 missense variant A/C snv 3.2E-05 3.5E-05 3
rs61749385
VWF
0.925 0.080 12 6019501 missense variant C/A;T snv 2
rs61749392
VWF
0.925 0.080 12 6019479 missense variant C/G snv 2
rs61749393
VWF
0.925 0.080 12 6019478 missense variant C/A;G snv 2
rs61750598
VWF
0.925 0.080 12 6018404 missense variant C/T snv 4.1E-04 1.7E-04 2
rs61749400
VWF
1.000 0.080 12 6019408 missense variant G/A;T snv 4.0E-06; 4.0E-06 1