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
rs61748497
VWF
0.851 0.080 12 6025624 missense variant A/G snv 4
rs61750072
VWF
0.925 0.080 12 6019297 missense variant C/A;T snv 4
rs61748477
VWF
0.925 0.080 12 6044361 missense variant G/A snv 8.0E-06 1.4E-05 3
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
rs61750071
VWF
0.882 0.080 12 6019298 missense variant G/A;T snv 4.0E-06 3
rs61750117
VWF
0.882 0.080 12 6018629 missense variant G/A;C;T snv 4.0E-06 3
rs61750584
VWF
0.882 0.080 12 6018535 missense variant A/G snv 3
rs61754010
VWF
0.882 0.080 12 6057995 missense variant T/C snv 4.0E-06 3
rs61754011
VWF
0.882 0.160 12 6057930 missense variant C/T snv 3
rs61751310
VWF ; ANO2
0.882 0.080 12 5949140 missense variant A/G snv 3
rs121964894
VWF
0.925 0.080 12 6036488 missense variant G/A snv 6.4E-05 4.2E-05 2
rs267607326
VWF
0.925 0.080 12 6022841 missense variant T/C snv 2
rs61749372
VWF
0.925 0.080 12 6019604 missense variant A/C;G 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
rs61749398
VWF
0.925 0.080 12 6019448 missense variant C/T snv 8.0E-06 2
rs61750101
VWF
0.925 0.080 12 6018877 missense variant A/C snv 2
rs61750577
VWF
0.925 0.080 12 6018628 missense variant C/A;T snv 2
rs61750579
VWF
0.925 0.080 12 6018598 missense variant A/T snv 2
rs61750581
VWF
0.925 0.080 12 6018581 missense variant A/G snv 2