ClinVar Miner

Submissions for variant NM_000593.6(TAP1):c.615A>G (p.Pro205=)

dbSNP: rs1770850860
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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 RCV001453924 SCV001657634 likely benign MHC class I deficiency 2019-05-13 criteria provided, single submitter clinical testing

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