ClinVar Miner

Submissions for variant NM_001378183.1(PIEZO2):c.1201-19C>G

gnomAD frequency: 0.05645  dbSNP: rs7241307
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000253148 SCV000313894 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001689909 SCV001912049 benign not provided 2018-07-09 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001689909 SCV002427734 benign not provided 2025-01-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001689909 SCV005248935 benign not provided criteria provided, single submitter not provided

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