ClinVar Miner

Submissions for variant NM_001085458.2(CTNND1):c.483C>T (p.Asp161=)

gnomAD frequency: 0.33696  dbSNP: rs10896644
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001638436 SCV001850059 benign not provided 2021-05-04 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001658347 SCV001876381 benign Blepharocheilodontic syndrome 2 2021-07-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001638436 SCV005324310 benign not provided criteria provided, single submitter not provided

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