ClinVar Miner

Submissions for variant NM_001290043.2(TAP2):c.493+19T>C

gnomAD frequency: 0.00001  dbSNP: rs773430770
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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 RCV002114634 SCV002446536 likely benign MHC class I deficiency 2022-03-02 criteria provided, single submitter clinical testing

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