ClinVar Miner

Submissions for variant NM_000593.6(TAP1):c.438G>A (p.Ala146=)

gnomAD frequency: 0.00190  dbSNP: rs78410191
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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 RCV000536948 SCV000642041 benign MHC class I deficiency 2025-01-23 criteria provided, single submitter clinical testing

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