ClinVar Miner

Submissions for variant NM_001290043.2(TAP2):c.687T>G (p.Leu229=)

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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 RCV003830227 SCV004631238 likely benign MHC class I deficiency 2023-11-16 criteria provided, single submitter clinical testing

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