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F2

—Coagulation Factor II

Chromosome: 11

Location: 11:46719079-46768566

OMIM: 176930

Ensembl: ENSG00000180210

Official·OMIM:176930 Official·ENSG00000180210

Encodes prothrombin protein. G20210A mutation causes thrombophilia.

Treatment Roadmap — F2

Preclinical

Phase 1

1 trial

Phase 2

2 trial

Phase 3

Approved

Clinical trials have approximately 10% success rate. This roadmap shows the current status, not guaranteed outcomes.

Associated Diseases

Prothrombin G20210A Mutation

Autosomal DominantPrevalence: 1/50hematologic

Official·OMIM:176930

Summary

Clinical Trial

Approved Therapy

Registered Variant