rs137852242, F9

N. diseases: 1
Source: UNIPROT ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Hemophilia B
CUI: C0008533
Disease: Hemophilia B
53 1.000 0.080 X 139551220 missense variant G/A;T snv 6.5E-05 0.700 0