ClinVar Miner

Submissions for variant NM_003190.5(TAPBP):c.747A>T (p.Pro249=)

dbSNP: rs2150961711
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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 RCV002071078 SCV002323365 likely benign MHC class I deficiency 2021-07-15 criteria provided, single submitter clinical testing

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