ClinVar Miner

Submissions for variant NM_001142864.4(PIEZO1):c.3433G>A (p.Val1145Met)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003740553 SCV004562676 uncertain significance not provided 2023-10-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003740553 SCV004637488 benign not provided 2023-12-01 criteria provided, single submitter clinical testing

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