ClinVar Miner

Submissions for variant NM_000165.5(GJA1):c.852T>G (p.Pro284=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002942464 SCV003271780 likely benign Oculodentodigital dysplasia, autosomal recessive 2022-07-25 criteria provided, single submitter clinical testing

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