ClinVar Miner

Submissions for variant NM_000528.4(MAN2B1):c.2924-4C>T

dbSNP: rs767564979
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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 RCV001424829 SCV001627432 likely benign Deficiency of alpha-mannosidase 2024-11-30 criteria provided, single submitter clinical testing

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