ClinVar Miner

Submissions for variant NM_002470.4(MYH3):c.4647+27G>A

gnomAD frequency: 0.01783  dbSNP: rs73281077
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000243566 SCV000308937 likely benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001709538 SCV001937692 benign not provided 2019-11-15 criteria provided, single submitter clinical testing

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