ClinVar Miner

Submissions for variant NM_012120.3(CD2AP):c.1632+89G>T

dbSNP: rs114654393
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001769742 SCV002004647 likely benign not provided 2020-03-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001769742 SCV005226085 likely benign not provided criteria provided, single submitter not provided

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