Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 1
rs111033613
F8
0.925 0.080 X 154928668 missense variant G/A;T snv 1
rs111033614
F8
1.000 0.080 X 154928667 missense variant C/T snv 1.1E-05 1.9E-05 1
rs111033615
F8
1.000 0.080 X 154904004 missense variant C/T snv 1
rs111033616
F8
1.000 0.080 X 154966065 missense variant A/T snv 1
rs1160914716
F8
1.000 0.080 X 154904392 missense variant T/A snv 1
rs1168919288
F8
1.000 0.080 X 154906458 missense variant C/G;T snv 1
rs1189348665
F8
1.000 0.080 X 154966663 missense variant A/G snv 1
rs1190563629
F8
1.000 0.080 X 154902121 missense variant C/A snv 1
rs1208703993
F8
1.000 0.080 X 154969540 missense variant C/T snv 1
rs1218576358
F8
1.000 0.080 X 154931627 missense variant C/T snv 1
rs1234456704
F8
1.000 0.080 X 154966463 missense variant A/G snv 1
rs1240470740
F8
1.000 0.080 X 154966004 missense variant G/A;C snv 1
rs1253524555
F8
1.000 0.080 X 154953969 missense variant T/A snv 1
rs1258333672
F8
1.000 0.080 X 154966101 missense variant T/A snv 1
rs1261929809
F8
1.000 0.080 X 155022410 missense variant C/T snv 1
rs1263565590
F8
1.000 0.080 X 154905005 missense variant C/G;T snv 1
rs1267586059
F8
1.000 0.080 X 154896187 missense variant C/T snv 1
rs1269117966
F8
1.000 0.080 X 154961075 missense variant C/T snv 1
rs1281943689
F8
1.000 0.080 X 154993074 missense variant A/G snv 1
rs1290383918
F8
0.925 0.080 X 154904505 missense variant C/A snv 1
rs1296842178
F8
1.000 0.080 X 154997069 missense variant C/T snv 9.5E-06 1
rs1299810903
F8
1.000 0.080 X 154953992 missense variant G/T snv 1
rs1304348198
F8
1.000 0.080 X 154966016 missense variant C/T snv 1
rs1305924233
F8
1.000 0.080 X 154931629 missense variant T/A;G snv 1