Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6025
rs6025
F5
43 0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 0.900 1.000 16 1997 2019
dbSNP: rs899127658
rs899127658
F2
82 0.547 0.720 11 46739084 missense variant G/A;C snv 0.100 1.000 15 1999 2019
dbSNP: rs2066865
rs2066865
FGG
10 0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 0.860 0.900 10 2011 2019
dbSNP: rs1799963
rs1799963
F2
25 0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 0.730 1.000 8 2012 2019
dbSNP: rs2036914
rs2036914
F11
5 0.882 0.160 4 186271327 intron variant T/C snv 0.57 0.830 1.000 5 2011 2019
dbSNP: rs2289252
rs2289252
F11 ; F11-AS1
4 1.000 0.040 4 186286227 non coding transcript exon variant C/T snv 0.35 0.740 1.000 5 2013 2019
dbSNP: rs78707713
rs78707713
TSPAN15
2 1.000 0.120 10 69485520 intron variant T/C snv 8.5E-02 0.710 0.800 5 2015 2020
dbSNP: rs2519093
rs2519093
ABO
16 0.882 0.200 9 133266456 intron variant T/C snv 0.820 1.000 4 2011 2019
dbSNP: rs529565
rs529565
ABO
13 0.851 0.120 9 133274084 intron variant C/T snv 0.800 1.000 4 2011 2016
dbSNP: rs2227589
rs2227589
SERPINC1
3 0.925 0.120 1 173917078 intron variant C/T snv 9.6E-02 0.030 1.000 3 2013 2019
dbSNP: rs2420371
rs2420371
F5
4 1 169522317 intron variant G/A snv 0.95 0.700 1.000 3 2009 2012
dbSNP: rs3756008
rs3756008
F11
2 4 186264231 upstream gene variant A/T snv 0.36 0.810 1.000 3 2011 2014
dbSNP: rs4253417
rs4253417
F11
3 4 186277851 intron variant T/C;G snv 0.800 1.000 3 2011 2019
dbSNP: rs505922
rs505922
ABO
34 0.689 0.520 9 133273813 intron variant C/T snv 0.800 1.000 3 2009 2012
dbSNP: rs579459
rs579459 		28 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 0.800 1.000 3 2011 2019
dbSNP: rs6427196
rs6427196
F5
3 1.000 0.080 1 169511985 3 prime UTR variant C/G;T snv 0.800 1.000 3 2011 2013
dbSNP: rs687289
rs687289
ABO
15 1.000 0.120 9 133261703 intron variant A/G snv 0.800 1.000 3 2011 2019
dbSNP: rs687621
rs687621
ABO
18 0.851 0.240 9 133261662 intron variant G/A;C snv 0.800 1.000 3 2011 2013
dbSNP: rs925451
rs925451
F11
2 4 186266415 intron variant G/A snv 0.34 0.710 1.000 3 2010 2012
dbSNP: rs1018827
rs1018827
F5
2 1 169544768 intron variant A/G snv 0.92 0.800 1.000 2 2011 2012
dbSNP: rs10737547
rs10737547 		2 1 169506814 intergenic variant A/G snv 0.93 0.700 1.000 2 2011 2012
dbSNP: rs10886430
rs10886430
GRK5
3 10 119250744 intron variant A/G snv 8.8E-02 0.700 1.000 2 2019 2019
dbSNP: rs1208134
rs1208134
CCDC181
2 1 169459706 intron variant C/T snv 0.93 0.700 1.000 2 2011 2012
dbSNP: rs1208135
rs1208135
CCDC181
2 1 169454860 intron variant A/G;T snv 0.700 1.000 2 2011 2012
dbSNP: rs1208327
rs1208327
NME7
2 1 169327626 intron variant C/G;T snv 0.700 1.000 2 2011 2012