ClinVar Miner

Submissions for variant NM_014975.3(MAST1):c.4356T>C (p.Pro1452=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV005143807 SCV005765047 likely benign not provided 2024-08-27 criteria provided, single submitter clinical testing

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