ClinVar Miner

Submissions for variant NM_001332.4(CTNND2):c.708C>T (p.Ser236=)

gnomAD frequency: 0.00045  dbSNP: rs766633367
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000910472 SCV001055340 likely benign not provided 2018-02-17 criteria provided, single submitter clinical testing
GeneDx RCV000910472 SCV002004756 likely benign not provided 2020-11-30 criteria provided, single submitter clinical testing

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