ClinVar Miner

Submissions for variant NM_001290043.2(TAP2):c.105G>A (p.Leu35=)

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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 RCV005155154 SCV005783913 likely benign MHC class I deficiency 2024-02-06 criteria provided, single submitter clinical testing

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