ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.3853+21C>T

gnomAD frequency: 0.00548  dbSNP: rs45584435
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Preventiongenetics, part of Exact Sciences RCV000168895 SCV000303226 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001575327 SCV001802295 likely benign not provided 2018-06-26 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV000168895 SCV001926888 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV000168895 SCV001958232 benign not specified no assertion criteria provided clinical testing

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