ClinVar Miner

Submissions for variant NM_000593.6(TAP1):c.1904-14C>T

gnomAD frequency: 0.00009  dbSNP: rs550493302
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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 RCV001909752 SCV002183359 likely benign MHC class I deficiency 2023-12-09 criteria provided, single submitter clinical testing

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