Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72661131
MBL2
0.742 0.480 10 52771739 upstream gene variant A/G snv 7.6E-04 15
rs562962093
MBL2
0.742 0.520 10 52771740 upstream gene variant T/C snv 7.0E-06 13
rs549591993
F7
0.776 0.400 13 113105794 5 prime UTR variant C/A snv 4.0E-04 2.8E-05 12
rs563558831
CYP2B6
0.776 0.320 19 40991226 upstream gene variant T/C snv 7.0E-06 11
rs549858786
IL1B
0.790 0.320 2 112836807 5 prime UTR variant T/A snv 10
rs17231520
CETP
0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 9
rs587745372
GJA5 ; LOC102723321
0.851 0.240 1 147773383 upstream gene variant T/A snv 2.8E-05 7
rs371045754
F9
0.882 0.200 X 139530726 upstream gene variant A/C snv 5.5E-06 1.9E-05 4
rs766182641
AK3
0.882 0.080 9 4719292 missense variant A/G snv 4.0E-06 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
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
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