ClinVar Miner

Submissions for variant NM_001290043.2(TAP2):c.648C>T (p.Tyr216=)

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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 RCV005082054 SCV005710780 likely benign MHC class I deficiency 2024-10-15 criteria provided, single submitter clinical testing

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