ClinVar Miner

Submissions for variant NM_001854.4(COL11A1):c.897+207A>G

gnomAD frequency: 0.01464  dbSNP: rs58786692
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001592211 SCV001822533 likely benign not provided 2018-07-08 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001592211 SCV005259212 likely benign not provided criteria provided, single submitter not provided

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