ClinVar Miner

Submissions for variant NM_002470.4(MYH3):c.5796+32del

dbSNP: rs147333978
Minimum review status: Collection method:
Minimum conflict level:
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 RCV000252154 SCV000308956 likely benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001660227 SCV001881057 benign not provided 2021-04-03 criteria provided, single submitter clinical testing

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