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: rs1018827
rs1018827
F5
2 1 169544768 intron variant A/G snv 0.92 0.700 1.000 1 2012 2012
dbSNP: rs10737547
rs10737547
2 1 169506814 intergenic variant A/G snv 0.93 0.700 1.000 1 2012 2012
dbSNP: rs10800427
rs10800427
1 1 169303213 non coding transcript exon variant A/C;T snv 0.96 0.700 1.000 1 2012 2012
dbSNP: rs10800428
rs10800428
1 1 169303215 non coding transcript exon variant G/A;T snv 0.96 0.700 1.000 1 2012 2012
dbSNP: rs10800448
rs10800448
1 1 169491168 non coding transcript exon variant A/G snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs114101204
rs114101204
1 1 169056816 intron variant G/A snv 1.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs114964168
rs114964168
1 1 169063639 intron variant C/T snv 1.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs1200063
rs1200063
1 1 169345192 intron variant T/C snv 0.95 0.700 1.000 1 2012 2012
dbSNP: rs1208134
rs1208134
2 1 169459706 intron variant C/T snv 0.93 0.700 1.000 1 2012 2012
dbSNP: rs1208135
rs1208135
2 1 169454860 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1208327
rs1208327
2 1 169327626 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1209731
rs1209731
2 1 169355555 intron variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs144737447
rs144737447
1 1 169191220 intron variant C/T snv 1.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs16861990
rs16861990
2 1 169165889 intron variant A/C snv 5.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs1894692
rs1894692
2 1 169498416 non coding transcript exon variant G/A snv 0.98 0.700 1.000 1 2012 2012
dbSNP: rs2213868
rs2213868
F5
1 1 169552315 intron variant G/A snv 0.95 0.700 1.000 1 2012 2012
dbSNP: rs2227246
rs2227246
1 1 169238941 intron variant C/T snv 0.98 0.700 1.000 1 2012 2012
dbSNP: rs2420371
rs2420371
F5
4 1 169522317 intron variant G/A snv 0.95 0.700 1.000 1 2012 2012
dbSNP: rs2420372
rs2420372
F5
2 1 169528818 intron variant A/G snv 0.95 0.700 1.000 1 2012 2012
dbSNP: rs2678166
rs2678166
1 1 169465789 3 prime UTR variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs3917693
rs3917693
1 1 169620132 intron variant C/T snv 3.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs4264045
rs4264045
1 1 169501510 downstream gene variant T/G snv 0.95 0.700 1.000 1 2012 2012
dbSNP: rs4656682
rs4656682
1 1 169494280 non coding transcript exon variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs4656683
rs4656683
1 1 169494281 non coding transcript exon variant T/C snv 0.80 0.700 1.000 1 2012 2012
dbSNP: rs6009
rs6009
F5
3 1.000 0.080 1 169529596 intron variant T/A;C snv 0.94 0.700 1.000 1 2012 2012