ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.3627+49C>T

gnomAD frequency: 0.26401  dbSNP: rs3729802
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 RCV000251341 SCV000303194 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001668422 SCV001889740 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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