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: rs1306658513
rs1306658513
F9
1.000 0.080 X 139561922 missense variant G/C snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B 		0.700 0