ClinVar Miner

Submissions for variant NC_000006.12:g.32853730A>G

gnomAD frequency: 0.00002  dbSNP: rs1329303922
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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 RCV001405085 SCV001607001 likely benign MHC class I deficiency 2023-02-13 criteria provided, single submitter clinical testing

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