Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs375422404
rs375422404
Entrez Id: 2160;285441
Gene Symbol: F11;F11-AS1
F11;F11-AS1
CUI: C0015523
Disease:
Hereditary Factor XI Deficiency
T 0.700 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749 2019
dbSNP: rs375422404
rs375422404
Entrez Id: 2160;285441
Gene Symbol: F11;F11-AS1
F11;F11-AS1
CUI: C0015523
Disease:
Hereditary Factor XI Deficiency
T 0.700 CausalMutation CLINVAR