Source: BEFREE ×
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 7
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 2
rs387906475
F9
0.882 0.080 X 139530843 missense variant G/A snv 2
rs387906482
F9
1.000 0.080 X 139561716 missense variant T/C snv 9.4E-06 2
rs753654616
F9
0.925 0.080 X 139561530 missense variant A/G snv 2
rs773084111
AK3
1.000 0.080 9 4713088 missense variant C/A snv 8.0E-06 7.0E-06 1
rs137852428
F8
0.925 0.080 X 154953961 missense variant G/A snv 2.2E-05 9.5E-06 1
rs137852227
F9
0.925 0.080 X 139537144 stop gained C/T snv 1
rs137852237
F9
1.000 0.080 X 139551112 missense variant C/A;T snv 5.5E-06 1
rs137852248
F9
1.000 0.080 X 139561565 stop gained C/A;T snv 1
rs137852249
F9
0.882 0.080 X 139561566 missense variant G/A snv 1
rs144314232
F9
1.000 0.080 X 139548430 synonymous variant G/A snv 5.5E-06 9.5E-06 1
rs147567879
F9
1.000 0.080 X 139561733 missense variant T/G snv 4.9E-05 1
rs750703108
HNF4A
1.000 0.080 20 44401424 missense variant G/A snv 2.0E-05 1.4E-05 1