ACTIONABILITY KNOWLEDGE REPOSITORY ACTIONABILITY CURATION INTERFACE

Pediatric Summary Report Secondary Findings in Pediatric Subjects Non-diagnostic, excludes newborn screening & prenatal testing/screening P Current Version Rule-Out Dashboard Release History Status (Pediatric): Incomplete (Consensus scoring is Incomplete) Curation Status (Pediatric): Released 1.0.4 Status (Adult): Passed (Consensus scoring is Complete) A

GENE/GENE PANEL: TTR
Condition: Hereditary transthyretin-related amyloidosis
Mode(s) of Inheritance: Autosomal Dominant
Actionability Assertion
Gene Condition Pairs(s)
Final Assertion
TTR0007100 (familial amyloid neuropathy)
N/A - Insufficient evidence: early rule-out
NOTICE
The 'Stage 2 Summary Report' is not available because as of the most recent update,
this gene-disease pair did not pass the Stage 1 Rule-Out survey.
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