ClinVar Miner

Submissions for variant NM_003190.5(TAPBP):c.333C>G (p.Pro111=)

gnomAD frequency: 0.00001  dbSNP: rs561857093
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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 RCV000917006 SCV001062266 benign MHC class I deficiency 2024-01-17 criteria provided, single submitter clinical testing

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