F11, coagulation factor XI, 2160

N. diseases: 100; N. variants: 139
Disease: Hereditary Factor XI Deficiency ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786204724
rs786204724
Entrez Id: 2160;285441
Gene Symbol: F11;F11-AS1
F11;F11-AS1
CUI: C0015523
Disease:
Hereditary Factor XI Deficiency 		A 0.700 GeneticVariation CLINVAR Revisiting the molecular epidemiology of factor XI deficiency: nine new mutations and an original large 4qTer deletion in western Brittany (France). 22159456 2012