ClinVar Miner

Submissions for variant NM_001290043.2(TAP2):c.222C>A (p.Pro74=)

dbSNP: rs2229526
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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 RCV000534017 SCV000642021 benign MHC class I deficiency 2024-01-28 criteria provided, single submitter clinical testing

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