Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs137852226
rs137852226
F9
1.000 0.080 X 139537139 missense variant A/T snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B 		0.800 1.000 2 2012 2013