ClinVar Miner

Submissions for variant NM_001378183.1(PIEZO2):c.7349+8G>A

gnomAD frequency: 0.03315  dbSNP: rs57838670
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000243705 SCV000313926 benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000957723 SCV001104538 benign not provided 2025-01-29 criteria provided, single submitter clinical testing
GeneDx RCV000957723 SCV001870086 benign not provided 2018-07-09 criteria provided, single submitter clinical testing

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