ClinVar Miner

Submissions for variant NM_014975.3(MAST1):c.1641G>A (p.Val547=)

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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 RCV002761125 SCV003010812 likely benign not provided 2022-08-16 criteria provided, single submitter clinical testing

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