ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.1436A>C (p.Asn479Thr)

dbSNP: rs727504236
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics, Academic Medical Center RCV001700657 SCV001921723 uncertain significance not provided no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001700657 SCV001929103 uncertain significance not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001700657 SCV001974135 uncertain significance not provided no assertion criteria provided clinical testing

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