ClinVar Miner

Submissions for variant NM_017780.4(CHD7):c.2835+24A>T

gnomAD frequency: 0.00081  dbSNP: rs201381395
Minimum review status: Collection method:
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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 RCV000247409 SCV000312965 likely benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001689882 SCV001910834 benign not provided 2020-10-20 criteria provided, single submitter clinical testing

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