ClinVar Miner

Submissions for variant NM_003190.5(TAPBP):c.177C>T (p.Asp59=)

dbSNP: rs1562701808
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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 RCV001398512 SCV001600285 likely benign MHC class I deficiency 2019-02-25 criteria provided, single submitter clinical testing

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