Source: UNIPROT ×
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: rs1410080079
rs1410080079
F9
1 1.000 0.080 X 139537120 missense variant G/A snv 0.700 0
dbSNP: rs757996262
rs757996262
F9
1 1.000 0.080 X 139562030 missense variant C/T snv 3.3E-05 8.6E-05 0.700 0
dbSNP: rs767828752
rs767828752
F9
1 1.000 0.080 X 139561982 missense variant G/A snv 0.700 0