ClinVar Miner

Submissions for variant NM_000593.6(TAP1):c.1050+15T>C

gnomAD frequency: 0.00019  dbSNP: rs372875467
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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 RCV002204117 SCV002491360 likely benign MHC class I deficiency 2023-10-24 criteria provided, single submitter clinical testing

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