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: rs10516487
rs10516487
BANK1
11 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs1060499784
rs1060499784
F8
1 1.000 0.080 X 154930646 stop gained C/T snv 0.700 0
dbSNP: rs111033613
rs111033613
F8
3 0.925 0.080 X 154928668 missense variant G/A;T snv 0.800 1.000 22 1989 2013
dbSNP: rs111033614
rs111033614
F8
2 1.000 0.080 X 154928667 missense variant C/T snv 1.1E-05 1.9E-05 0.800 1.000 22 1989 2013
dbSNP: rs111033615
rs111033615
F8
1 1.000 0.080 X 154904004 missense variant C/T snv 0.810 1.000 23 1989 2013
dbSNP: rs111033616
rs111033616
F8
1 1.000 0.080 X 154966065 missense variant A/T snv 0.800 1.000 22 1989 2013
dbSNP: rs1160914716
rs1160914716
F8
1 1.000 0.080 X 154904392 missense variant T/A snv 0.700 0
dbSNP: rs1168919288
rs1168919288
F8
1 1.000 0.080 X 154906458 missense variant C/G;T snv 0.700 0
dbSNP: rs1189348665
rs1189348665
F8
1 1.000 0.080 X 154966663 missense variant A/G snv 0.700 1.000 20 1989 2002
dbSNP: rs1190563629
rs1190563629
F8
1 1.000 0.080 X 154902121 missense variant C/A snv 0.700 0
dbSNP: rs1208703993
rs1208703993
F8
1 1.000 0.080 X 154969540 missense variant C/T snv 0.700 1.000 20 1989 2002
dbSNP: rs1218576358
rs1218576358
F8
1 1.000 0.080 X 154931627 missense variant C/T snv 0.700 0
dbSNP: rs1234456704
rs1234456704
F8
1 1.000 0.080 X 154966463 missense variant A/G snv 0.700 0
dbSNP: rs1240470740
rs1240470740
F8
1 1.000 0.080 X 154966004 missense variant G/A;C snv 0.700 0
dbSNP: rs1253524555
rs1253524555
F8
1 1.000 0.080 X 154953969 missense variant T/A snv 0.700 0
dbSNP: rs1258333672
rs1258333672
F8
1 1.000 0.080 X 154966101 missense variant T/A snv 0.700 0
dbSNP: rs1261929809
rs1261929809
F8
1 1.000 0.080 X 155022410 missense variant C/T snv 0.700 0
dbSNP: rs1263565590
rs1263565590
F8
1 1.000 0.080 X 154905005 missense variant C/G;T snv 0.700 0
dbSNP: rs1267586059
rs1267586059
F8
1 1.000 0.080 X 154896187 missense variant C/T snv 0.700 0
dbSNP: rs1269117966
rs1269117966
F8
1 1.000 0.080 X 154961075 missense variant C/T snv 0.700 0
dbSNP: rs1281943689
rs1281943689
F8
1 1.000 0.080 X 154993074 missense variant A/G snv 0.700 1.000 20 1989 2002
dbSNP: rs1290383918
rs1290383918
F8
2 0.925 0.080 X 154904505 missense variant C/A snv 0.700 1.000 20 1989 2002
dbSNP: rs1296842178
rs1296842178
F8
1 1.000 0.080 X 154997069 missense variant C/T snv 9.5E-06 0.700 1.000 20 1989 2002
dbSNP: rs12979860
rs12979860
IFNL4
84 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.010 1.000 1 2014 2014
dbSNP: rs1299810903
rs1299810903
F8
1 1.000 0.080 X 154953992 missense variant G/T snv 0.700 0