Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 14
rs61748497
VWF
0.851 0.080 12 6025624 missense variant A/G snv 4
rs61750595
VWF
0.882 0.080 12 6018443 stop gained G/A;T snv 5.6E-05 3
rs61750612
VWF
0.882 0.080 12 6013544 stop gained G/A;T snv 1.6E-05 3
rs61753997
VWF
0.882 0.080 12 6075392 missense variant G/A snv 2.8E-05; 8.0E-06 4.2E-05 3
rs62643632
VWF
0.925 0.080 12 6044298 frameshift variant G/-;GG delins 6.3E-05 3
rs61750598
VWF
0.925 0.080 12 6018404 missense variant C/T snv 4.1E-04 1.7E-04 2
rs61750630
VWF
0.925 0.080 12 5981988 missense variant C/A snv 2
rs61751296
VWF
0.925 0.080 12 5969337 stop gained G/A snv 1.6E-05 1.4E-05 2
rs61751305
ANO2 ; VWF
1.000 0.080 12 5949823 missense variant C/T snv 8.0E-06 1
rs61750086
VWF
1.000 0.080 12 6019050 stop gained G/C;T snv 1
rs61750615
VWF
1.000 0.080 12 5994484 missense variant G/A;T snv 1.3E-02 1
rs61751298
VWF
1.000 0.080 12 5969304 missense variant T/A snv 4.0E-06 7.0E-06 1
rs61753998
VWF
1.000 0.080 12 6075386 missense variant A/G;T snv 1
rs62643626
VWF
1.000 0.080 12 6071322 missense variant C/A snv 1
rs958629333
VWF
1.000 0.080 12 6121245 missense variant A/G snv 1
rs61751306
VWF ; ANO2
1.000 0.080 12 5949195 missense variant A/C snv 1