ClinVar Miner

Submissions for variant NM_002473.6(MYH9):c.2871C>T (p.Ser957=)

gnomAD frequency: 0.00073  dbSNP: rs374840260
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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 RCV000243282 SCV000309040 likely benign not specified criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000725873 SCV000340144 uncertain significance not provided 2016-04-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000725873 SCV001028047 benign not provided 2025-01-15 criteria provided, single submitter clinical testing
GeneDx RCV000725873 SCV001814443 likely benign not provided 2020-07-25 criteria provided, single submitter clinical testing

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