ClinVar Miner

Submissions for variant NM_000593.6(TAP1):c.990C>T (p.Val330=)

dbSNP: rs1468233071
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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 RCV002217664 SCV002375882 likely benign MHC class I deficiency 2022-04-07 criteria provided, single submitter clinical testing

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