Genomics England
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Panels
Genes and Entities
SERPINC1
serpin family C member 1
OMIM:
107300
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Panel
Mode of inheritance
Details
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Thrombophilia with a likely monogenic cause
R-numbers:
R97
Signed-off version 2.2
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Thrombophilia due to antithrombin III deficiency, OMIM:613118