rs121965064, F11

N. diseases: 3
Source: ALL
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.
Hereditary Factor XI Deficiency
CUI: C0015523
Disease: Hereditary Factor XI Deficiency
119 0.925 0.080 4 186280258 missense variant T/C snv 1.1E-03 6.4E-04 0.810 1.000 26 1989 2019
Blood Coagulation Disorders
CUI: C0005779
Disease: Blood Coagulation Disorders
31 0.925 0.080 4 186280258 missense variant T/C snv 1.1E-03 6.4E-04 0.010 1.000 1 2008 2008
Factor XI Deficiency
CUI: C4321502
Disease: Factor XI Deficiency
9 0.925 0.080 4 186280258 missense variant T/C snv 1.1E-03 6.4E-04 0.010 1.000 1 2008 2008