Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
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
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
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
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 11
rs1800386
VWF
0.851 0.120 12 6018667 missense variant T/C snv 2.7E-03 2.3E-03 5
rs766182641
AK3
0.882 0.080 9 4719292 missense variant A/G snv 4.0E-06 3
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
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
rs387906475
F9
0.882 0.080 X 139530843 missense variant G/A snv 3
rs748641905
MCFD2
0.882 0.080 2 46905501 missense variant A/T snv 3
rs111033614
F8
1.000 0.080 X 154928667 missense variant C/T snv 1.1E-05 1.9E-05 2
rs1290383918
F8
0.925 0.080 X 154904505 missense variant C/A snv 2
rs137852360
F8
0.925 0.080 X 154837676 missense variant C/A;G;T snv 2