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: rs121965066
rs121965066
Entrez Id: 2160
Gene Symbol: F11
F11
CUI: C0015523
Disease:
Hereditary Factor XI Deficiency 		A 0.700 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749 2019
dbSNP: rs121965066
rs121965066
Entrez Id: 2160
Gene Symbol: F11
F11
CUI: C0015523
Disease:
Hereditary Factor XI Deficiency 		A 0.700 CausalMutation CLINVAR