ClinVar Miner

Submissions for variant NM_001290043.2(TAP2):c.1144-6T>C

dbSNP: rs9461814
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001434057 SCV001636858 likely benign MHC class I deficiency 2024-01-13 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004707598 SCV005225649 likely benign not provided criteria provided, single submitter not provided

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