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: rs13412535
rs13412535
5 2 224010157 intron variant G/A snv 0.17 0.700 1.000 1 2017 2017
dbSNP: rs1557570
rs1557570
F5
1 1 169538606 intron variant G/T snv 0.30 0.700 1.000 1 2017 2017
dbSNP: rs1568119
rs1568119
1 8 33385679 intron variant C/T snv 4.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs184905639
rs184905639
1 8 33229938 upstream gene variant G/A snv 3.8E-03 0.700 1.000 1 2017 2017
dbSNP: rs200393053
rs200393053
1 8 32736709 intron variant T/-;TT delins 0.700 1.000 1 2017 2017
dbSNP: rs4841899
rs4841899
2 9 134532566 intron variant T/C snv 0.32 0.700 1.000 1 2017 2017
dbSNP: rs635634
rs635634
22 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs80271436
rs80271436
1 9 133022383 downstream gene variant G/A snv 4.7E-02 0.700 1.000 1 2017 2017