ClinVar Miner

Submissions for variant NM_001142864.4(PIEZO1):c.769G>A (p.Ala257Thr)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002599313 SCV003496758 benign not provided 2022-07-13 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV002599313 SCV003812904 uncertain significance not provided 2022-11-18 criteria provided, single submitter clinical testing

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