ClinVar Miner

Submissions for variant NC_000006.12:g.32853805A>C

gnomAD frequency: 0.00061  dbSNP: rs148176741
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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 RCV000642372 SCV000764041 likely benign MHC class I deficiency 2024-02-01 criteria provided, single submitter clinical testing

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