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: 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: rs4524
rs4524
F5
3 1 169542517 missense variant T/C snv 0.28 0.24 0.710 1.000 3 2015 2019
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
3 10 119250744 intron variant A/G snv 8.8E-02 0.700 1.000 2 2019 2019
dbSNP: rs1208134
rs1208134
2 1 169459706 intron variant C/T snv 0.93 0.700 1.000 2 2011 2012
dbSNP: rs1208135
rs1208135
2 1 169454860 intron variant A/G;T snv 0.700 1.000 2 2011 2012
dbSNP: rs1208327
rs1208327
2 1 169327626 intron variant C/G;T snv 0.700 1.000 2 2011 2012
dbSNP: rs12445050
rs12445050
3 16 81837364 intron variant C/T snv 9.6E-02 0.700 1.000 2 2019 2019
dbSNP: rs16861990
rs16861990
2 1 169165889 intron variant A/C snv 5.5E-02 0.800 1.000 2 2011 2012
dbSNP: rs1894692
rs1894692
2 1 169498416 non coding transcript exon variant G/A snv 0.98 0.700 1.000 2 2011 2012
dbSNP: rs2066864
rs2066864
FGG
2 4 154604543 3 prime UTR variant G/A snv 0.26 0.800 1.000 2 2011 2019
dbSNP: rs2420370
rs2420370
F5
1 1 169521154 intron variant G/C snv 0.95 0.700 1.000 2 2011 2012
dbSNP: rs2420372
rs2420372
F5
2 1 169528818 intron variant A/G snv 0.95 0.700 1.000 2 2011 2012
dbSNP: rs2842700
rs2842700
1 1 207108804 intron variant C/A;G snv 0.12 0.700 1.000 2 2019 2019
dbSNP: rs3756009
rs3756009
F11
2 4 186264957 upstream gene variant A/G snv 0.32 0.700 1.000 2 2011 2012
dbSNP: rs4253399
rs4253399
F11
2 4 186266940 intron variant T/G snv 0.30 0.800 1.000 2 2011 2013
dbSNP: rs4602861
rs4602861
1 8 105578478 intron variant A/G;T snv 0.700 1.000 2 2015 2017
dbSNP: rs545971
rs545971
ABO
8 9 133267960 intron variant T/A;C snv 0.700 1.000 2 2011 2012
dbSNP: rs612169
rs612169
ABO
10 9 133268030 intron variant G/A snv 0.700 1.000 2 2011 2012
dbSNP: rs630014
rs630014
ABO
9 9 133274306 intron variant G/A;C snv 0.700 1.000 2 2011 2012
dbSNP: rs6427194
rs6427194
F5
2 1 169511883 downstream gene variant T/A snv 0.91 0.700 1.000 2 2011 2012