ClinVar Miner

Submissions for variant NM_003190.5(TAPBP):c.1068C>T (p.Ser356=)

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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 RCV002587256 SCV002941024 likely benign MHC class I deficiency 2022-04-16 criteria provided, single submitter clinical testing

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