Source: CURATED

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 14
rs1799963
F2
0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 10
rs137852435
F8
0.925 0.080 X 154931641 missense variant G/A snv 1.7E-05 3
rs28935499
F8
0.925 0.080 X 154966525 missense variant C/A;T snv 3
rs886039906
F8
1.000 0.080 X 154929022 frameshift variant -/TTGGTTAT ins 3.3E-05 3
rs137852247
F9
0.925 0.080 X 139560852 missense variant G/A snv 3
rs137852249
F9
0.882 0.080 X 139561566 missense variant G/A snv 3
rs137852254
F9
0.882 0.080 X 139561710 missense variant C/T snv 3
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 2
rs111033613
F8
0.925 0.080 X 154928668 missense variant G/A;T snv 2
rs111033614
F8
1.000 0.080 X 154928667 missense variant C/T snv 1.1E-05 1.9E-05 2
rs137852358
F8
0.882 0.080 X 154861758 missense variant C/A;T snv 2
rs137852360
F8
0.925 0.080 X 154837676 missense variant C/A;G;T snv 2
rs137852394
F8
0.925 0.080 X 154992996 missense variant C/T snv 2
rs137852405
F8
0.925 0.080 X 154969405 missense variant A/G snv 2
rs137852414
F8
0.925 0.080 X 154961120 stop gained C/A;T snv 2
rs137852416
F8
0.925 0.080 X 154957073 missense variant G/A snv 2
rs137852424
F8
0.925 0.080 X 154953991 stop gained G/A;T snv 1.1E-05 2
rs137852428
F8
0.925 0.080 X 154953961 missense variant G/A snv 2.2E-05 9.5E-06 2
rs137852436
F8
0.925 0.080 X 154931623 missense variant C/T snv 5.5E-06 2
rs137852461
F8
0.925 0.080 X 154863151 missense variant C/T snv 2
rs137852465
F8
0.925 0.080 X 154863124 missense variant C/A;T snv 5.5E-06 2
rs137852469
F8
0.925 0.080 X 154860588 missense variant C/A snv 2
rs137852472
F8
0.925 0.080 X 154837697 missense variant G/A snv 2
rs1490417405
F8
0.925 0.080 X 154903950 missense variant C/T snv 9.5E-06 2