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: rs1462083784
rs1462083784
THBD
1 20 23049251 missense variant C/T snv 7.3E-06 0.010 1.000 1 2002 2002
dbSNP: rs387906482
rs387906482
F9
2 1.000 0.080 X 139561716 missense variant T/C snv 9.4E-06 0.010 1.000 1 2000 2000
dbSNP: rs776339896
rs776339896
F10 ; F10-AS1
1 13 113129584 missense variant G/A snv 4.0E-06 0.010 1.000 1 2002 2002