ClinVar Miner

Submissions for variant NM_000038.6(APC):c.358A>C (p.Arg120=)

dbSNP: rs876659470
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000218846 SCV000275981 uncertain significance Hereditary cancer-predisposing syndrome 2015-05-25 criteria provided, single submitter clinical testing There is insufficient or conflicting evidence for classification of this alteration.

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