ClinVar Miner

Submissions for variant NM_000593.6(TAP1):c.1378-4C>G

gnomAD frequency: 0.00001  dbSNP: rs746948561
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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 RCV000811939 SCV000952231 likely benign MHC class I deficiency 2023-08-11 criteria provided, single submitter clinical testing

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