Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
rs1799963
F2
0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 25
rs111033613
F8
0.925 0.080 X 154928668 missense variant G/A;T snv 3
rs137852358
F8
0.882 0.080 X 154861758 missense variant C/A;T snv 3
rs1290383918
F8
0.925 0.080 X 154904505 missense variant C/A snv 2
rs137852403
F8
0.925 0.080 X 154969438 missense variant C/A;T snv 2
rs137852442
F8
0.925 0.080 X 154904998 missense variant C/T snv 2
rs782127226
F8
0.925 0.080 X 154928962 missense variant C/A snv 4.4E-05 2
rs3754689
LCT
0.925 0.080 2 135833176 missense variant C/A;G;T snv 4.8E-05; 0.24 2
rs781901822
F8
1.000 0.080 X 154928683 missense variant C/T snv 5.6E-06 1
rs782198570
F8
1.000 0.080 X 154861818 missense variant T/C snv 2.2E-05 9.5E-06 1