ClinVar Miner

Submissions for variant NM_000593.6(TAP1):c.1155C>T (p.Gly385=)

gnomAD frequency: 0.00005  dbSNP: rs139907578
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000642379 SCV000764048 likely benign MHC class I deficiency 2024-01-03 criteria provided, single submitter clinical testing

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