ClinVar Miner

Submissions for variant NM_000593.6(TAP1):c.1746T>C (p.Ala582=)

dbSNP: rs2127387213
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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 RCV001403863 SCV001605748 likely benign MHC class I deficiency 2019-04-26 criteria provided, single submitter clinical testing

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