ClinVar Miner

Submissions for variant NM_000073.3(CD3G):c.162A>G (p.Thr54=)

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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 RCV003052816 SCV003445032 likely benign Combined immunodeficiency due to CD3gamma deficiency 2023-07-28 criteria provided, single submitter clinical testing

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