ClinVar Miner

Submissions for variant NM_001142864.4(PIEZO1):c.5340C>T (p.Asp1780=)

dbSNP: rs372159659
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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 RCV001810804 SCV002048400 likely benign not provided 2021-09-09 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001810804 SCV004266436 benign not provided 2023-10-13 criteria provided, single submitter clinical testing

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