Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121964894
VWF
0.925 0.080 12 6036488 missense variant G/A snv 6.4E-05 4.2E-05 1
rs267607342
VWF
1.000 0.080 12 6018799 missense variant A/G snv 1
rs372028373
VWF
1.000 0.080 12 6019466 missense variant C/A;T snv 7.2E-05 1
rs41276738
VWF
0.807 0.080 12 6034812 missense variant C/T snv 3.4E-03 3.7E-03 1
rs61748476
VWF
1.000 0.080 12 6044370 missense variant C/T snv 1
rs61748477
VWF
0.925 0.080 12 6044361 missense variant G/A snv 8.0E-06 1.4E-05 1
rs61748497
VWF
0.851 0.080 12 6025624 missense variant A/G snv 1
rs61749370
VWF
0.882 0.080 12 6019621 missense variant G/A;T snv 8.0E-04; 2.8E-04 1
rs61749371
VWF
1.000 0.080 12 6019616 missense variant G/A;C;T snv 1
rs61749372
VWF
0.925 0.080 12 6019604 missense variant A/C;G snv 1
rs61749384
VWF
0.882 0.080 12 6019502 missense variant G/A snv 1
rs61749387
VWF
0.882 0.080 12 6019496 missense variant G/A snv 1
rs61749392
VWF
0.925 0.080 12 6019479 missense variant C/G snv 1
rs61749393
VWF
0.925 0.080 12 6019478 missense variant C/A;G snv 1
rs61749397
VWF
0.807 0.080 12 6019472 missense variant C/G;T snv 4.0E-06 1
rs61749398
VWF
0.925 0.080 12 6019448 missense variant C/T snv 8.0E-06 1
rs61749403
VWF
0.882 0.080 12 6019396 missense variant C/A;G;T snv 4.0E-06 1
rs61750071
VWF
0.882 0.080 12 6019298 missense variant G/A;T snv 4.0E-06 1
rs61750072
VWF
0.925 0.080 12 6019297 missense variant C/A;T snv 1
rs61750088
VWF
1.000 0.080 12 6019040 missense variant G/A;C snv 1.6E-05 1
rs61750089
VWF
1.000 0.080 12 6019036 missense variant G/A;T snv 1
rs61750101
VWF
0.925 0.080 12 6018877 missense variant A/C snv 1
rs61750117
VWF
0.882 0.080 12 6018629 missense variant G/A;C;T snv 4.0E-06 1
rs61750577
VWF
0.925 0.080 12 6018628 missense variant C/A;T snv 1
rs61750579
VWF
0.925 0.080 12 6018598 missense variant A/T snv 1